Below you will find third-party sites and resources. If you have a favorite resource that's not included in the list, please let us know.
European Sterile Products Confederation (ESPC)
- A3P France
The association A3P was founded in 1986 to meet the needs of the pharmaceutical industry, biotechnological and biomedical response to rapidly changing technologies and processes production and control.
Place of exchange and advanced knowledge between specialists, the Association relies on its A3P international network of members.
It is through events (conferences, scientific meetings, forums) qu'A3P assured leadership in its field.
Email contact: firstname.lastname@example.org
- AEFI Spain
The Association has a national level and is governed by the General Assembly, composed of all tenured members. Between meetings, the governing body is the Board of Governors, which consists of the President of the Association, two vice presidents, secretary, treasurer, 3 members from other Catalan section 3 of the center section, as well as the national voice of Industry General Council of Official Colleges of Pharmacists.
Email Contact: email@example.com
- R3Nordic Scandivnavia
R3 Nordic is a non-profit association and a well established network for research, education, product development, and production within the R3 technology – Cleanroom technique and Cleanrooms – in the Nordic countries.
Email contact: firstname.lastname@example.org
The Association of the British Pharmaceutical Industry (ABPI) represents innovative research-based biopharmaceutical companies, large, medium and small, leading an exciting new era of biosciences in the UK.
Our industry, a major contributor to the economy of the UK, brings life-saving and life-enhancing medicines to patients. Our members supply 90 per cent of all medicines used by the NHS, and are researching and developing over two-thirds of the current medicines pipeline, ensuring that the UK remains at the forefront of helping patients prevent and overcome diseases.
The ABPI is recognised by government as the industry body negotiating on behalf of the branded pharmaceutical industry for statutory consultation requirements including the pricing scheme for medicines in the UK.
- Association of British Healthcare Industries
ABHI is the industry association for the medical technology sector in the UK.
ABHI’s purpose is to promote the rapid adoption of medical technologies to ensure optimum patient outcomes throughout the UK and in key global markets.
With over 250 company members ABHI is the voice of the medical technology sector, championing industry to the NHS, Government, regulators and stakeholders.
Pharmig is the influential forum for microbiology in the pharmaceutical, healthcare and allied industries. It provides a focus for continuing professional development and a unique opportunity for the exchange of microbiological information. Pharmig is a non-profit making organisation, established in 1991, that represents the interests of individuals working in, have responsibility for, or work alongside microbiology.
- Royal Pharmaceutical Society
The Pharmaceutical Society of Great Britain was founded on April 15th 1841 by a group of leading London chemists and druggists.
- Royal Society of Chemistry
The RSC is the largest organisation in Europe for advancing the chemical sciences. Supported by a worldwide network of members and an international publishing business, our activities span education, conferences, science policy and the promotion of chemistry to the public.
- The Scottish Society for Contamination Control
The objectives of S2C2 as laid down in its constitution are:
To advance the education of the public in matters relating to the practice and science of contamination control.
To assist in the development of contamination control for the benefit of the public, not only for the advancement of the education of the public but also for the furtherance of their health.
To assist in the standardisation of effective methods of contamination control.
- British Pharmacopoeia
The British Pharmacopoeia 2014, the only official source of British pharmaceutical standards
- European Medicines Agency
The European Medicines Agency is a decentralised agency of the European Union, located in London. The Agency is responsible for the scientific evaluation of medicines developed by pharmaceutical companies for use in the European Union.
- Food Drug Agency
FDA is responsible for:
Protecting the public health by assuring that foods are safe, wholesome, sanitary and properly labeled; human and veterinary drugs, and vaccines and other biological products and medical devices intended for human use are safe and effective.
Protecting the public from electronic product radiation.
Assuring cosmetics and dietary supplements are safe and properly labeled.
Regulating tobacco products.
Advancing the public health by helping to speed product innovations.
Helping the public get the accurate science-based information they need to use medicines, devices, and foods to improve their health.
FDA’s responsibilities extend to the 50 United States, the District of Columbia, Puerto Rico, Guam, the Virgin Islands, American Samoa, and other U.S. territories and possessions.
- Irish Medicines Board
The objective of the IMB is to ensure in so far as possible, consistent with current medical and scientific knowledge, the quality, safety and efficacy of medicines available in Ireland and to participate in systems designed to do that throughout the European Union. Before a medicine can be authorised for use, an application must be made to the IMB and this must contain all of the necessary data supporting its quality, safety and efficacy.
- Medicines and Healthcare Products Regulatory Agency
MHRA protect and improve the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research.
- Pharmaceutical Inspection Co-operation Scheme
The Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (jointly referred to as PIC/S) are two international instruments between countries and pharmaceutical inspection authorities, which provide together an active and constructive co-operation in the field of GMP.