Tripartite Conferences

In September 1958, two years after the British government ruling, representatives of Porton Down met their American and Canadian counterparts at the Thirteenth Tripartite Conference on Toxicological Warfare, held in Canada. It can be assumed that all three countries, although two were now committed to purely defensive research, pooled their information. But the summary of the conference also records that ... 

The specific series of experiments in which Maddison died was suggested by the Tripartite Conference and authorized by the Air Ministry on 12 February 1953. It was agreed that we had the facilities we should... 

Image 29. William ( BiU ) LadeU with members of the Tripartite Conference Source IWM, Photographic Collection, no date. O Imperial War Museums (F. 794)-The man standing in the middle is William Ladell. 

At the end of 1958, members of the Thirteenth Tripartite Conference, held in Ottawa and Suflield in Canada, confirmed that there was an urgent... 

In recent years, regulatory authorities and industry associations have undertaken several important initiatives to promote international harmonization of regulatory requirements. These efforts are designed to enhance harmonization and are committed to seeking scientifically based harmonized technical procedures for pharmaceutical development. These efforts are undertaken under the auspices of the International Conference on Harmonization (ICH), which is organized to provide an opportunity for tripartite... 

ICH Steering Committee, 1997, ICH Harmonised Tripartite guideline, Impurities Guideline for Residual Solvents, Q3C. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. 

International Conference on Harmonisation, ICH Harmonised Tripartite Guideline, Validation of Analytical Procedures Methodology, November 1996. 

International Conference on Harmonization. Organization of the common technical document for the registration of pharmaceuticals for human use, in Harmonized Tripartite Guideline, ICH, 2002. 

It was agreed, from the start, that the focus for discussions of tripartite harmonisation should be an international conference or series of conferences. The Steering Committee recognised the importance of ensuring that the process of harmonisation is carried out in an open and transparent manner and that ICH discussions and recommendations are presented in open forums. 

Since 1999, all embryo-fetal toxicity studies on new drugs are per-formedaccordingto theinternational Conference onHarmonisation (ICH) Harmonised Tripartite Guideline on Detection of Toxicity to Reproduction for Medicinal Products (8) (see Chapter 1). 

Tripartite guidelines issued by the International Conference on Harmonisation (ICH) can be found at http //www.ich.org/ products/guidelines/safety/article/safety-guidelines.html. 

International conference on harmonisation of technical requirements for registration of pharmaceuticals for human use (2005) ICH harmonised tripartite guideline. Detection of toxicity to reproduction for medicinal products 8c toxicity to male fertility, S5(r2) current step 4 version parent guideline dated 24 June 1993 (addendum dated 9 November 2000 incorporated in November 2005)... 

To facilitate worldwide registration and marketing of the drug product, more and more, drug research, development, and production are performed at multiple sites located in different countries. A tripartite organization, known as the International Conference on Flarmonization (ICFI), was established in 1991 to address the possibil-... 

Grimm W. (1998), Extension of International Conference on Harmonization tripartite guideline for stability testing of new drug substances and products to countries of climatic zones III and IV, Drug Dev. Ind. Pharm., 24,313-325. 

International Conference on Harmonization (ICH) Steering Committee (1994), ICH harmonized tripartite guideline, Stability testing of new drug substances and products, ICH, Geneva. 

---