Product News

Version 4.2 of cGARD is now available

Yet another update to our ever growing database of regulations is now available. This time we have added regulations from USA, EU, UK, and Japan along with providing an update on all 21 CFR regulations (revised on 1st April 2007).

The new version includes following additional regulations:

USA:

21 CFR Part: 10, 19-21, 25, 60, 70-71, 73-74, 80-82, 99, 201-202, 207, 250, 290, 299, 300, 310, 315-316, 895, 1401-1405

EU:Eudralex

 Volume 4: Annex 20 - Quality Risk Management

Japan:

Pharmaceutical Administration and Regulations in Japan English Regulatory Information Task Force, Japan, Pharmaceutical Manufacturers Association - March 2006

UK:

S.I. 2005-2753 - Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 2005 - October 2005

S.I. 2005-2753 - Explanatory Note - October 2005

S.I. 2005-2753 (Schedule 5) - Procedural Provisions Relating to the Grant Renewal, Variation, Revocation and Suspension of Certificates of Registration - October 2005

S.I. 2005-2753 (Schedule 6) - Offences, Penalties etc. - October 2005

S.I. 2005-2753 (Schedule 7) - Transitional Provisions - October 2005

S.I. 2005-2753 (Schedule) - Consequential Amendments of the Act and Other Regulations - October 2005