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The Center for Biologics Evaluation and Research (CBER) within the United States Food and Drug Administration (FDA) regulates the collection of blood and blood components used for transfusion or for the manufacture of pharmaceuticals derived from blood and blood components, such as clotting factors, and establishes standards for the products themselves.
AABB (formerly known as the American Association of Blood Banks) is an international association representing individuals and institutions involved in activities related to transfusion and cellular therapies, including transplantation medicine.
Joe Chaffin started this site in 1998 as a way to help pathology residents and my fellow pathologists learn more about Blood Banking in a relaxed environment.
Canadian Blood Services is a not-for-profit, charitable organization whose sole mission is to manage the blood and blood products supply for Canadians.
A web site dedicated to the exchange of accurate blood information and health information related to your blood. Nothing here is to be viewed as medical advice.
Society for the Advancement of Blood Management - To improve patient outcomes through optimal blood management. Blood management is the appropriate provision and use of blood, its components and derivatives, and strategies to reduce or avoid the need for a blood transfusion.
Network for Advancement of Transfusion Alternatives, an international network of medical practitioners, researchers, and opinion leaders from a wide variety of medical and scientific disciplines who are dedicated to helping their peers learn more about recent advances in blood conservation and transfusion alternatives.
Physicians for the Advancement of Tranfusion Medicine develop and maintain a new medical voice for transfusion medicine. Our voice will be evidence-based, derived through consensus and will represent the medical interest of patients and patient care.
Association of Donor Recruitment Professionals is committed to being a leader in providing education, development and resources for the donor recruitment profession.
American Society for Clinical Pathology has been the leader in pathology and laboratory medicine. The societys influence has guided the evolution and maturation of this medical specialty. ASCP is unique among pathology organizations in that its inclusive membership unites pathologists and laboratory professionals to advance the profession.
College of American Pathologists, the leading organization of board-certified pathologists, serves patients, pathologists, and the public by fostering and advocating excellence in the practice of pathology and laboratory medicine.
Clinical Laboratory Standards Institute (formerly NCCLS) is a global, nonprofit, standards-developing organization that promotes the development and use of voluntary consensus standards and guidelines within the health care community.
American Society of Hematology is the worlds largest professional society concerned with the causes and treatments of blood disorders. The mission of the Society is to further the understanding, diagnosis, treatment, and prevention of disorders affecting the blood, bone marrow, and the immunologic, hemostatic and vascular systems, by promoting research, clinical care, education, training, and advocacy in hematology.
The Armed Services Blood Program plays a key role in providing quality blood products for Service members and their families in both peace and war. As a joint operation among the military services (Army, Navy, Air Force), the ASBP has many components working together to collect, process, store, distribute, and transfuse blood worldwide.
The American Society for Clinical Laboratory Science (ASCLS), as the preeminent organization for clinical laboratory science practitioners, provides dynamic leadership and vigorously promotes all aspects of clinical laboratory science practice, education and management to ensure excellent, accessible cost-effective laboratory services for the consumers of health care.
American Society for Blood and Marrow Transplantation is a national professional association that promotes advancement of the field of blood and bone marrow transplantation. ASBMT members are both in clinical practice and in research.
The Australian & New Zealand Society of Blood Transfusion (ANZSBT) comprises members from diverse scientific, technical and medical backgrounds working within the areas of Blood Tranfusion and Transfusion Medicine within Australia and New Zealand.
International Council for Commonality in Blood Banking Automation, Inc (ICCBBA) enhances safety for patients by managing the ISBT 128 international information standard for use in transfusion and transplantation.
The International Society of Blood Transfusion (ISBT) is a scientific society of world renown, founded in 1935 and bringing together professionals involved in blood transfusion and transfusion medicine from more than 95 countries.
he Blood Banks Association of New York State is a non-profit, professional organization dedicated to improving transfusion medicine within the State by fostering education and the exchange of ideas among professionals in the field.
CBBS supports Health Care Professionals involved in Transfusion Medicine by providing continuing education, strengthening professional relationships, responding to regional issues and encouraging collaborative efforts.
The Heart of America Association of Blood Banks is a nonprofit, professional organization dedicated to improving transfusion medicine by fostering the exchange of information and bringing education opportunities to blood bank and transfusion medicine professionals. The HAABB hosts two annual meetings for the Kansas City and St. Louis areas.
The Indiana State Association of Blood Banks is an educational network among individual blood bankers and institutional blood banks in the state of Indiana.
The Mid-Atlantic Association of Blood Banks, serving an organization of members from Delaware, Maryland, Washington, DC and Virginia. MAABB is dedicated to the continued education and involvement of its members in all topics of blood banking.
The North Carolina Association of Blood Banks serves as an association of laboratory technologists, physicians, nurses, and other interested individuals in North Carolina with experience and duties in the realm of blood banking, immunohematology and blood transfusion.
The Ohio Association of Blood Banks mission is to promote education, professional growth and technical expertise in Blood Banking, Transfusion Medicine and related disciplines and to provide the highest standard of service and care to all of our customers, including, but not limited to, patients, donors, and peers.
South Central Association of Blood Banks (SCABB) is a nonprofit organization consisting of eight states assigned to three districts. The districts include District I, Texas; District II, Arizona, Colorado, New Mexico, Nevada, and Oklahoma; District III, Arkansas, Louisiana, and Mississippi.
Tennessee Association of Blood Banks is a not-for-profit organization of blood bank and transfusion medicine professionals and other individuals working in this field.
The Wisconsin Association of Blood Banks is committed to providing current information and to generating a forum for discussion of mutual concerns for all individuals in Wisconsin who are interested in the field of blood banking.
The
European Group for Blood and Marrow Transplantation
is a non-profit organisation based in Maastricht, The Netherlands, that was established in 1974 in order to allow scientists and physicians involved in clinical bone marrow transplantation to share their experience and develop co-operative studies.
The Center for Biologics Evaluation and Research (CBER) within the United States Food and Drug Administration (FDA) regulates human gene therapy products - products that introduce genetic material into the body to replace faulty or missing genetic material, thus treating or curing a disease or abnormal medical condition.
Association for Harmonization of Cellular Therapy Accreditation
members commit themselves to the harmonisation of their respective standards with the objective of creating a single set of quality, safety and professional requirements for cellular therapy including haematopoietic stem cell (HSC) transplantation.
The
American Society for Histocompatibility and Immunogenetics
is an international society of professionals dedicated to advancing the science, education, and application of immunogenetics and transplant immunology.
Foundation for the Accredication of Cellular Therapy
establishes standards for high quality medical and laboratory practice in cellular therapies. FACT is a non-profit corporation co-founded by the International Society for Cellular Therapy (ISCT) and the American Society of Blood and Marrow Transplantation (ASBMT) for the purposes of voluntary inspection and accreditation in the field of cellular therapy.
International Society for Cellular Therapy
is the global forum and resource for developing and supporting innovative cellular therapies through communication, education, and training, thus furthering clinical based investigation for the benefit of patients.
The Joint Accreditation Committee-ISCT & EBMT is a non-profit body established in 1998 for the purposes of assessment and accreditation in the field of haematopoietic stem cell (HSC) transplantation.
The
American Society of Gene & Cell Therapy
is a professional non-profit medical and scientific organization dedicated to the understanding, development and application of genetic and cellular therapies and the promotion of professional and public education in the field.
The
European Society of Gene and Cell Therapy
promotes basic and clinical research in gene therapy, cell therapy, and genetic vaccines by facilitating education, the exchange of information and technology and by serving as a professional adviser to stakeholder communities and regulatory bodies in Europe.
The
Alliance for Cancer Gene Therapy
is in the right place at the right time, leading the way for innovative research using cells and genes as "medicine."
The
Association of Genetic Technologists, founded in 1975, is a non-profit professional organization established to promote cooperation and exchange of information among those engaged in classical cytogenetics, molecular and biochemical genetics, and to stimulate interest in genetics as a career.
The
Austrian Network for Gene Therapy
is a multidiscipliniary working group aimed at bringing together scientists, clinicians and industry active in the field of gene therapy.
The aim of the
British Society for Gene Therapy
is to accelerate scientific progress and promote ethical and efficient transfer of gene- and cell-based technologies from the laboratory into the clinic.
The
Finnish Gene Therapy Society
aims to foster the exchange of ideas between research groups and individual scientists, to organize scientific meetings and training courses and to inform general public about basic aspects and recent developments of gene therapy.
The
International Society for Stem Cell Research
is an independent, nonprofit organization formed in 2002 to foster the exchange of information on stem cell research.
The
Israeli Society of Gene Therapy
was established in May 2002 and is a non profit organization. The Society is an organizational tool for research and clinical development in the field of Gene Therapy in the broad sense of the term.
European Network for the Advancement of Clinical Gene Transfer and Therapy: EC funded network of excellence fostering interaction of all stakeholders in the field in order to facilitate and help harmonise Ethical, Quality, Safety, Efficacy and Regulatory issues.
The aims of the
Swedish Society for Gene Therapy
are to promote basic and clinical research in gene therapy, to foster education and the exchange of information and technology related to gene transfer and therapy, and to inform general public about basic aspects and recent developments of gene therapy, and to serve as a professional adviser to the regulatory bodies in Sweden and Europe.
Gene Therapy Net
is the web resource for patients and professionals interested in gene therapy. The objectives of Gene Therapy Net are to be the information resource for basic and clinical research in gene therapy, cell therapy, and genetic vaccines, and to serve as a network in the exchange of information and news related to above areas.
The Center for Biologics Evaluation and Research (CBER) within the United States Food and Drug Administration (FDA) regulates human cells or tissue intended for implantation, transplantation, infusion, or transfer into a human recipient.
California Department of Public Health - Laboratory Field Services - To ensure quality standards in clinical and public health laboratories and laboratory scientists through licensing, examination, inspection, education, and proficiency testing.
Delaware Health and Social Services - Division of Public Health - Public Health Laboratory
Manages oversight of clinical laboratories affiliated with blood and tissue banks.
Texas Department of State Health Services - Drugs and Medical Devices Group
Registration of distributors with locations in Texas - not specific to tissue banks.
The
American Association of Tissue Banks
is dedicated to ensuring that human tissues intended for transplantation are safe and free of infectious disease, of uniform high quality, and available in quantities sufficient to meet national needs.
the
United Network for Organ Sharing
is a non-profit, scientific and educational organization that administers the nation's only Organ Procurement and Transplantation Network (OPTN), established by the U.S. Congress in 1984.
The
Organ Procurement and Transplantation Network
is the unified transplant network established by the United States Congress under the National Organ Transplant Act (NOTA) of 1984.
The
Association of Organ Procurement Organizations
represents and serves OPOs through advocacy, support, and development of activities that will maximize the availability of organs and tissues and enhance the quality, effectiveness, and integrity of the donation process.
Donate Life America, formerly the Coalition on Donation, was founded by the transplant community in 1992 to educate the public about organ, eye and tissue donation and avoid duplication of effort.
The
American Board for Transplant Certification
is an independent, not-for-profit organization whose purpose is to award a voluntary, non-governmental certification credential, "Certified Clinical Transplant Coordinator (CCTC)"; "Certified Procurement Transplant Coordinator (CPTC)," or "Certified Clinical Transplant Nurse (CCTN)" to qualified transplant coordinators or transplant nurses who have successfully passed the certification examination, which represents a standard of competence.
University of Michigan TransWeb's mission has been constant since its inception in 1994 to the present, to provide information about donation and transplantation to the general public in order to improve organ and tissue procurement efforts worldwide and to provide transplant patients and families worldwide with information specifically dealing with transplant-related issues and concern.
The
International Pediatric Transplant Association
is dedicated to promoting the advancement of the science and practice of transplantation in children worldwide.
The
International Society for Organ Preservation
will be the source for education for all interested acquiring knowledge in the fast expanding field of organ preservation.
Asia Pacific Association of Tissue Banking
was established with special interest in tissue banking, to encourage research in tissue banking in the Asia Pacific region and to promote scientific and social interaction among its member.
The
Australasian Tissue Biotherapeutics Forum
is a not-for-profit organisation inaugurated in 2000. Its mission is to foster and promote best practice in the retrieval, preparation, storage and distribution of human tissue for transplantation throughout Australasia.
The
European Association of Tissue Banks
is an advocate for its members in all medical, scientific and other professional activities associated with tissue banking.
EUSTITE
is a 3 year project that has been funded by the European Union following the publication of 3 EU directives defining minimum standards of quality and safety for human tissues and cells that are applied to patients for therapeutic purposes.
The
American Society of Multicultural Health and Transplant Professionals
share ideas in meeting the common mission of increasing organ and tissue donation among minority communities.
The
European Transplant Coordinators Organization
was set up in 1983 to represent all those working as Transplant Coordinators in Europe and around the world to promote organ and tissue donation in all member countries.
The
International Transplant Nurses Society
is committed to the promotion of excellence in clinical transplant nursing through the provision of educational and professional growth opportunities, interdisciplinary networking, collaborative activities, and nursing research.
The
Centers for Disease Control and Prevention (CDC)
within the United States Department of Health and Human Services (DHHS) has been dedicated to protecting health and promoting quality of life through the prevention and control of disease, injury, and disability.
The
National Vaccine Information Center
is a national, non-profit educational organization founded in 1982. The oldest and largest consumer organization advocating the institution of vaccine safety and informed consent protections in the mass vaccination system, NVIC is responsible for launching the vaccine safety and informed consent movement in America in the early 1980's.
The
Allied Vaccine Group
is comprised of websites dedicated to presenting valid scientific information about the sometimes confusing subject of vaccines.
The
International Society for Vaccines
is an organization that engages, supports, and sustains the professional goals of a diverse membership in all areas relevant to vaccines.
The
Vaccine Adverse Event Reporting System
is a national vaccine safety surveillance program co-sponsored by the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA).
The
Brighton Collaboration
is an international voluntary collaboration to facilitate the development, evaluation, and dissemination of high quality information about the safety of human vaccines.
United States National Institutes of Health -
National Institute of Allergy and Infectious Diseases
- The mission of the Vaccine Research Center (VRC) is to conduct research that facilitates the development of effective vaccines for human disease. The primary focus of research is the development of vaccines for AIDS.
The
International Vaccine Institute
is an International Organization established at the initiative of the United Nations Development Programme under the Vienna Convention of 1969 and is an international center of research, training and technical assistance for vaccines needed in developing countries.
United Kingdom Xenotransplantation Interim Regulatory Authority
ceased to exist from 12 December 2006. This change follows a number of amendments to the statutory framework. Other Government Committees, Research Ethics Committees, and clinical governance arrangements are absorbing the functions.
Hyman, Phelps & McNamara, P.C. is the largest dedicated food and drug law firm in the country. Our niche practices in the areas of new drug development, controlled substances, advertising, and health care law complement our core FDA practice. Our knowledge of the laws and regulations governing drugs, medical devices, foods, dietary supplements, and cosmetics is unparalleled in breadth and depth.
The Massachusetts Medical Devices Journal is the online journal of the medical devices industry in the Commonwealth and New England, providing day-to-day coverage of the devices that save lives, the people behind them, and the burgeoning trends and developments within the industry.
Karin Gregory, an attorney who's spent more than 30 years in healthcare, is a founding partner at Furman Gregory LLC. The Massachusetts Medical Devices Journal is the online journal of the medical devices industry in the Commonwealth and New England.
The purpose of this Transparency Blog is to discuss various ways in which the Food and Drug Administration (FDA) could provide information to the public about whatFDA is doing, the bases for FDAs decisions, and the processes used to make agency decisions.
Former medical school professor, industrial scientist, professional recruiter, management consultant, entrepreneur and career development expert who has been around the block and wants to share his experiences to help others launch successful careers in the bioscience industry!
Blog of BII an Institute having thousands of program participants from more than 40 countries. BII is the training leader in emerging life science and pharma domains. Blog focus is on Bioinformatics, Biotechnology, Pharma Regulatory Affairs, Clinical Trials, Drug Design and Discovery, IPR, GMP
The Prinz Law Office specializes in providing world-class intellectual property counsel to clients in the high technology, life science, and e-commerce industries.
MARK SENAK, J.D. - Authority on regulatory aspects of communications and medical products, with particular emphasis on pre-approval communications; strategist to help pharma and biotech companies prepare best case for advisory committee approval; issues and crisis management.
Hyman, Phelps & McNamara, P.C. is the largest dedicated food and drug law firm in the country. Our niche practices in the areas of new drug development, controlled substances, advertising, and health care law complement our core FDA practice. Our knowledge of the laws and regulations governing drugs, medical devices, foods, dietary supplements, and cosmetics is unparalleled in breadth and depth.
MindPharm, LLC; a recruiting and resource firm dedicated to the bioscience community. The MindPharmNet Blog posts positions we are currently looking to fill, as well as generally interesting industry news.
A blog on Medical Devices, Biotechnology, Bioengineering, Healthcare, etc. Join me on discussions about devices, regulations, the FDA, policies, law and what not!
The Massachusetts Medical Devices Journal is the online journal of the medical devices industry in the Commonwealth and New England, providing day-to-day coverage of the devices that save lives, the people behind them, and the burgeoning trends and developments within the industry.
Karin Gregory, an attorney who's spent more than 30 years in healthcare, is a founding partner at Furman Gregory LLC. The Massachusetts Medical Devices Journal is the online journal of the medical devices industry in the Commonwealth and New England.
The purpose of this Transparency Blog is to discuss various ways in which the Food and Drug Administration (FDA) could provide information to the public about whatFDA is doing, the bases for FDAs decisions, and the processes used to make agency decisions.
Public Responsibility in Medicine and Research (PRIM&R - pronounced "prim-er") advances the highest ethical standards in the conduct of biomedical, social science, behavioral, and educational research.
This is a blog about human-subjects research ethics. It is written primarily by Nancy Walton, Ph.D., (with occasional postings by Chris MacDonald, Ph.D.)
Hyman, Phelps & McNamara, P.C. is the largest dedicated food and drug law firm in the country. Our niche practices in the areas of new drug development, controlled substances, advertising, and health care law complement our core FDA practice. Our knowledge of the laws and regulations governing drugs, medical devices, foods, dietary supplements, and cosmetics is unparalleled in breadth and depth.
The Nutritional and Dietary Supplement Law Blog is published jointly by Attorney Joel B. Rothman with the national firm of Arnstein & Lehr, LLP and NutriCompliance, a regulatory compliance firm providing solutions and consulting services to consumer health and dietary supplement businesses.
Hyman, Phelps & McNamara, P.C. is the largest dedicated food and drug law firm in the country. Our niche practices in the areas of new drug development, controlled substances, advertising, and health care law complement our core FDA practice. Our knowledge of the laws and regulations governing drugs, medical devices, foods, dietary supplements, and cosmetics is unparalleled in breadth and depth.
BOB COFFIELD - A health care lawyer practicing at Flaherty, Sensabaugh & Bonasso, PLLC. Focused on helping businesses and health care providers weave through a variety of state and federal health care regulations and assisting them in business transactions.
GREG PICHE is an attorney at Holland & Hart LLP where he specializes in healthcare law. This blog is dedicated to Healthcare Law issues in or affecting the Mountain West and the states in which we practice which include Montana, Idaho, Wyoming, Utah, Colorado, Nevada and New Mexico.
TOM MAYO [1] Director, Cary M. Maguire Center for Ethics and Public Responsibility (SMU); [2] Associate Professor, SMU/Dedman School of Law; [3] Adjunct Associate Professor, Internal Medicine, UT-Southwestern Medical School; [4] Of Counsel, Haynes and Boone, LLP
MindPharm, LLC; a recruiting and resource firm dedicated to the bioscience community. The MindPharmNet Blog posts positions we are currently looking to fill, as well as generally interesting industry news.
JAYNE E. JUVAN, Esq., an attorney affliliated withBenesch Friedlander Coplan & Aronoff, LLP,is a member of thefirm's Private Equity Practice Group and Health Care Practice Group.
Our strongest allies believe that there are many challenges in the pharma space that are bigger than just one company. Addressing and solving these problems and generating new opportunities requires collaborative discussion and debate across the entire industry.
This blog contains JIM BECK and MARK HERRMANN's personal views of various topics that arise in the defense of pharmaceutical and medical device product liability litigation.
MARK SENAK, J.D. - Authority on regulatory aspects of communications and medical products, with particular emphasis on pre-approval communications; strategist to help pharma and biotech companies prepare best case for advisory committee approval; issues and crisis management.
Hyman, Phelps & McNamara, P.C. is the largest dedicated food and drug law firm in the country. Our niche practices in the areas of new drug development, controlled substances, advertising, and health care law complement our core FDA practice. Our knowledge of the laws and regulations governing drugs, medical devices, foods, dietary supplements, and cosmetics is unparalleled in breadth and depth.
I always felt that there was not a venue to discuss design issues, enhancement requests, or just share FAQs. I want to encourage the development community to share their ideas and solutions.
Strategy, Regulatory, Innovation & Investment coverage from the industry's top publications. Highlights from The Gray Sheet, Medtech Insight, IN VIVO, Start-Up, The Silver Sheet and Strategic Transactions.
A blog on Medical Devices, Biotechnology, Bioengineering, Healthcare, etc. Join me on discussions about devices, regulations, the FDA, policies, law and what not!
Neracs team of medical device analysts will provide industry insights and analysis on marketplace activities and hot topics, including innovation progress and trends, rapidly developing technologies, intellectual property developments, compliance hurdles and commercial opportunities.
MDCI is a full-service contract research organization and consulting firm that helps emerging and established firms commercialize novel and innovative medical devices, in vitro diagnostics and combination products.
The Massachusetts Medical Devices Journal is the online journal of the medical devices industry in the Commonwealth and New England, providing day-to-day coverage of the devices that save lives, the people behind them, and the burgeoning trends and developments within the industry.
Karin Gregory, an attorney who's spent more than 30 years in healthcare, is a founding partner at Furman Gregory LLC. The Massachusetts Medical Devices Journal is the online journal of the medical devices industry in the Commonwealth and New England.
The purpose of this Transparency Blog is to discuss various ways in which the Food and Drug Administration (FDA) could provide information to the public about whatFDA is doing, the bases for FDAs decisions, and the processes used to make agency decisions.
A blog on Medical Devices, Biotechnology, Bioengineering, Healthcare, etc. Join me on discussions about devices, regulations, the FDA, policies, law and what not!
Neracs team of medical device analysts will provide industry insights and analysis on marketplace activities and hot topics, including innovation progress and trends, rapidly developing technologies, intellectual property developments, compliance hurdles and commercial opportunities.
Blog of BII an Institute having thousands of program participants from more than 40 countries. BII is the training leader in emerging life science and pharma domains. Blog focus is on Bioinformatics, Biotechnology, Pharma Regulatory Affairs, Clinical Trials, Drug Design and Discovery, IPR, GMP
This blog contains JIM BECK and MARK HERRMANN's personal views of various topics that arise in the defense of pharmaceutical and medical device product liability litigation.
MARK SENAK, J.D. - Authority on regulatory aspects of communications and medical products, with particular emphasis on pre-approval communications; strategist to help pharma and biotech companies prepare best case for advisory committee approval; issues and crisis management.
Hyman, Phelps & McNamara, P.C. is the largest dedicated food and drug law firm in the country. Our niche practices in the areas of new drug development, controlled substances, advertising, and health care law complement our core FDA practice. Our knowledge of the laws and regulations governing drugs, medical devices, foods, dietary supplements, and cosmetics is unparalleled in breadth and depth.
MindPharm, LLC; a recruiting and resource firm dedicated to the bioscience community. The MindPharmNet Blog posts positions we are currently looking to fill, as well as generally interesting industry news.
I always felt that there was not a venue to discuss design issues, enhancement requests, or just share FAQs. I want to encourage the development community to share their ideas and solutions.
The blog of Pharmaceutical Technology, the authoritative source of peer-reviewed research and expert analyses for scientists, engineers, and managers engaged in process development, manufacturing, formulation and drug delivery, API synthesis, analytical technology and testing, packaging, IT, outsourcing, and regulatory compliance in the pharmaceutical and biotechnology industries.
JOHN MACK - These are my personal opinions and do not represent the opinions of Pharma Marketing News. Read the newsletter for a more unbiased presentation of facts, product reviews and coverage of pharma industry conferences -- all based upon interviews with experts in the field of pharmaceutical marketing.
The purpose of this Transparency Blog is to discuss various ways in which the Food and Drug Administration (FDA) could provide information to the public about whatFDA is doing, the bases for FDAs decisions, and the processes used to make agency decisions.
Our strongest allies believe that there are many challenges in the pharma space that are bigger than just one company. Addressing and solving these problems and generating new opportunities requires collaborative discussion and debate across the entire industry.
Public Responsibility in Medicine and Research (PRIM&R - pronounced "prim-er") advances the highest ethical standards in the conduct of biomedical, social science, behavioral, and educational research.
This is a blog about human-subjects research ethics. It is written primarily by Nancy Walton, Ph.D., (with occasional postings by Chris MacDonald, Ph.D.)
Hyman, Phelps & McNamara, P.C. is the largest dedicated food and drug law firm in the country. Our niche practices in the areas of new drug development, controlled substances, advertising, and health care law complement our core FDA practice. Our knowledge of the laws and regulations governing drugs, medical devices, foods, dietary supplements, and cosmetics is unparalleled in breadth and depth.
Welcome to Sperm Bank Information from Xytex.com. We are a community sharing information on donor sperm banks and sperm donor donations for artificial insemination and in vitro fertilization. Join our discussion forums and talk about donor sperm bank clinics and programs worldwide.
ANIMAL PHARM IS A DAILY ELECTRONIC BUSINESS NEWS SERVICE, AND A FORTNIGHTLY NEWSLETTER, FOR ANYONE INTERESTED IN OR INVOLVED WITH THE ANIMAL HEALTH INDUSTRIES. AND THESE ARE THE THOUGHTS AND COMMENTS OF ITS PUBLISHER ON BOTH THE WORLD OF ANIMAL HEALTH AND THE BUSINESS OF B2B PUBLISHING.
The Association of Electrical and MEdical Imaging Equipment Manufacturers (formerly
National Electrical Manufacturers Association) - EICareers - Career Center
RAPS is committed to helping you succeed at every stage of your professional development. Regulatory professionals are highly skilled experts employed in industry, government and academia, and are responsible for guiding these healthcare products through the approval process and onto the market.
Staying competitive in the business world means getting new skills and knowledge on a continuing basis. American Management Association is a recognized leader in professional developmentand becoming an AMA Member is a great way to take advantage of our world-class seminars and many other valuable resources.
PMI serves practitioners and organizations with standards that describe good practices, globally recognized credentials that certify project management expertise, and resources for professional development, networking and community.
ACRP is the primary resource for clinical research professionals in the pharmaceutical, biotechnology and medical device industries, and those in hospital, academic medical centers and physician office settings.
The Society of Clinical Research Associates, Inc. is a non-profit, professional organization dedicated to the continuing education and development of clinical research professionals.
ClinicalTrials.gov is a registry of federally and privately supported clinical trials conducted in the United States and around the world. ClinicalTrials.gov gives you information about a trial's purpose, who may participate, locations, and phone numbers for more details.
MRM is one of the nation's leading providers of clinical research education and customized training to leading CROs; Pharmaceutical, Medical Device, and Biotechnology Companies; and Research sites and Universities. Many companies are currently using MRM's e-learning courses as a requirement for new employees or ongoing GCP/ICH training.
One-Source Web Portal Provides Global Regulatory Intelligence for Pharma and Medical Device Companies.
- Access hands-on knowledge from 200+ senior regulatory experts
- Search among national authorities documents of 75+ countries and regions
The Personal Care Products Council follows, identifies and obtains legal and regulatory documents from all over the world. These documents are translated into English, and added to the International Legal and Regulatory Database (IRDB).
IDRAC, the complete pharmaceutical regulatory intelligence solution from Thomson Reuters, equips your organization to stay fully up to date with the ever-changing requirements of governments and regulatory authorities around the world.
Master of Science in Bioscience Regulatory Affairs is intended for those students who know they want a career in Regulatory Affairs and intend to work specifically in the field. Students taking the MS in Biotechnology with a concentration in Regulatory Affairs are typically those more interested in bioscience, but would like a better understanding of the regulatory process.
Temple University School of Pharmacy was the first institution of higher learning to develop a masters program in Quality Assurance and Regulatory Affairs in 1968.
Master of Science in Regulatory Affairs - This degree program will provide a comprehensive background in regulatory science with the additional training and experience required of regulatory affairs professionals to address federal and state regulatory statutes and laws with emphasis on the Food and Drug Administration. The degree is offered through the collaboration of the College of Sciences and the College of Business Administration.
The MS in Regulatory Science is an intensive, interdisciplinary program designed to produce graduates whose backgrounds in biological, pharmaceutical and biomedical sciences are enhanced by the knowledge and skills needed to manage regulated biomedical products. Centered in the School of Pharmacy, the full-time or part-time program has an interdisciplinary, three-semester curriculum and relies on the participation of professionals from public and private sectors.
The campus-based or online Master of Science in Regulatory Affairs program for Drugs, Biologics, and Medical Devices is designed to educate and prepare RA professionals who will play a pivotal role in ensuring compliance with applicable laws and regulations in the strategic development and commercialization of health care products of their company.
Master of Science in Quality Assurance and Regulatory Science - An interdisciplinary professional program, the MQARS curriculum emphasizes applied science, leadership, and communication skills. Students explore concepts and problems in quality assurance and regulatory affairs that span life science industries, thus encouraging a cross-pollination of best practices and systems.
Master of Science in Clinical Research and Regulatory Administration - Career advancement opportunities abound for the effective clinical research professional at academic medical centers, research sites, and in pharmaceutical and medical device organizations. In response to the growing need for competent professionals in the industry.
St. Cloud State University Master of Science in Regulatory Affairs and Services (MS-RAS) provides not only a solid education in regulatory affairs but also training in related areas of clinical affairs, quality systems, and health care reimbursement -- areas of expertise also in high demand by this industry.
The Department of Pharmacy and Administrative Science (PAS) teaches students the knowledge, attitudes and skills required for contemporary clinical pharmacy practice. Students studying for the masters in pharmacy administration may specialize in Pharmaceutical Marketing and Regulatory Affairs/Quality Assurance. The Regulatory Affairs/Quality Assurance Program provides comprehensive knowlege for Regulatory Affairs (RA) and Quality Assurance (QA) professionals seeking employment or career advancement in pharmaceutical companies, hospitals, governmental agencies, health care organizations and academia.
Master of Science Degree in Pharmacy with an emphasis in Regulatory Affairs. This program is geared for Regulatory Affairs working professionals. As such, this program is designed to be taken on a part-time basis.
Bachelor of Science in Clinical Research. The Department of Clinical Research is headquartered in North Carolinas Research Triangle Park (RTP), and teaches classes at this campus and the Universitys Buies Creek campus.
Our Executive Master of Science in Clinical Research is well suited for several student populations, and classes are held in the evening to allow all of these students access to this degree program. First, students can enter this program having completed the Bachelor of Science in Clinical Research degree, or any other suitable undergraduate degree, and continue their education in clinical research.
Master of Bioscience - Clinical and Regulatory Affairs focus track provides an understanding of how the FDA and its international counterparts regulate the development of novel products including assessment of product quality, non-clinical and clinical evaluation.
Master of Science in Regulatory Affairs and Health Policy - The RAHP masters program can be completed in under two years, and is ideal for those interested in pursuing careers in regulatory affairs, product management, marketing, quality assurance & control, and manufacturing.
The Master of Science Degree in Health Product Regulation is designed for candidates with baccalaureate degrees in the sciences or who are currently working in the regulatory field (With permission of Director). Candidates for this program are those men and women who wish to advance in professional training or seek a career in the biotechnology, device, or pharmaceutical industries.
Pharmaceutical Sciences Graduate Program - Specialization in Pharmaceutics and Phamacokinetics - Design, development, production, evaluation and regulatory approval of pharmaceutical and self-care products as well as pharmacokinetic and pharmacodynamic studies using virtual, clinical, and preclinical data, often with an emphasis on population approaches.
Medical Technology Regulatory Affairs MSc - part-time. Cranfields qualification - in collaboration with The Organisation for Professionals in Regulatory Affairs (TOPRA) - combines TOPRAs long-standing experience and expertise with Cranfields strong academic reputation and its links to industry
Master of Drug Regulatory Affairs (MDRA). This postgraduate course started in the winter semester of 1999/2000 at the University of Bonn's Faculty of Mathematics and Natural Sciences. In its interdisciplinary approach it combines aspects of the pharmaceutical sciences, law and medicine.
Medicines Control Council - a statutory body that was established in terms of the Medicines and Related Substances Control Act, 101 of 1965, to oversee the regulation of medicines in South Africa.
Health Canada - Health Canada administers many pieces of legislation and develops and enforces regulations under this legislation affecting drugs and health products.
COFEPRIS - The Federal Commission for the Protection against Sanitary Risk (COFEPRIS) is a decentralized organ of the Department of Health with technical, administrative and operational autonomy, whose mission is to protect the population against sanitary risks, through sanitary regulation, control and promotion.
FDA - The Food and Drug Administration in the United States Department of Health and Human Services. The FDA is responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nations food supply, cosmetics, and products that emit radiation.
The Organization for Professionals in Regualtory Affairs
is the global organisation for Regulatory Affairs professionals and for those who have an interest in Regulatory Affairs in the healthcare sector.
Canadian Association of Professional Regulatory Affairs
is a non-profit association dedicated to providing information and education for regulatory affairs professionals in the health-care industry in Canada.
