Regulatory

CIRS RD Briefing 40 – Pharmacogenetics and pharmacogenomics in drug development

Summarised results of a survey carried out among pharmaceutical companies and regulatory agencies, by the CMR International Institute for Regulatory Science Pharmacogenetic (PGt) and pharmacogenomic (PGx) technologies are being [...]

2021-02-08T16:35:20+00:00December 2nd, 2003|Tags: |

CIRS RD Briefing 39 – Regulating personalised medicine

Highlights of the workshop "Regulating personalised medicine" organised by the CMR International Institute for Regulatory Science, Nutfield Priory, Surrey, UK, 14-15 April 2003 The unravelling of the human genome [...]

2026-01-05T16:57:16+00:00December 1st, 2003|Tags: , |

CIRS RD Briefing 38 – Risk management

Highlights of the CMR International institute Workshop on 'Risk Management: Identifying and Developing Effective Stakeholder Communication During Drug Development', held on 12-13 December 2002. Following a number of high [...]

2026-01-05T16:54:36+00:00June 1st, 2003|Tags: , , |

CIRS RD Briefing 37 – Adoption of ICH E5 in Asia Pacific

In 2001, CMR International conducted a study among pharmaceutical companies to evaluate their experience with regulatory authorities in Asia Pacific regarding the acceptance of foreign clinical data and adoption [...]

2025-03-20T16:43:30+00:00December 1st, 2002|Tags: , , |

CIRS RD Briefing 36 – Impact of ICH E5 guideline

The ICH E5 Guideline was introduced in February 1998 and subsequently implemented by the regulatory authorities of the USA, EU and Japan. The purpose of this guideline is to [...]

2025-03-20T16:43:18+00:00October 1st, 2002|Tags: , |
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