Practical Advice and Good Practices
Click on any of the following articles below to view published practice advice and good practice guidance:
- Risk-Adapted Approaches to the Management of Clinical Trials of Investigational Medicinal Products (Sep 2012)
- Frequently Asked Regulatory Questions About Investigational Medicinal Products (Sep 2012)
- Stability Testing – the Basics (Feb 2010)
- Accounting for VAT in Clinical Supplies (Mar 2009)
- Sourcing Placebos in Bulk: Making Use of Regulation 37 in SI 2004/1031 (Feb 2009)
- Common Reasons for Delays in CTA Applications (Jan 2009)
- Failing to Plan Trial Medication Early Can Cost the Entire Trial (Oct 2008)
