We routinely conduct gap assessments for clients to identify any shortcomings between regulatory agency requirements and current Good Manufacturing Practices (cGMPs) and a company’s current operations. The gap assessment is often a good preemptive measure to gauge any areas of deficiency, and focuses efforts and resources on areas requiring improvement.
Our assessments identify gaps in your existing quality systems and provide recommendations for how to best address these gaps. If the expertise or skills necessary to implement these improvements are not present within your organization, we have a wide range of consultants who are subject matter experts and who can address the most complex problems with tailored, practical solutions to meet your specific needs.
For more information about NSF Pharma Biotech services in quality systems and compliance in the U.S., email email@example.com or call +1 202.822.1850.
For more information about NSF Pharma Biotech services in quality systems and compliance in Europe, email firstname.lastname@example.org or call +44 1751 432 999.
When: September 27 - October 1, 2014 Where: Austin, TX Booth: 418 NSF Participation Elaine C. Messa, RAC, FRAPS, President,...
- 3 months ago
The long-awaited Qualified Persons template for declarations concerning Good Manufacturing Practice compliance of active substances and the accompanying guidance have...
- 4 months ago
On July 1, 2014, the Irish Medicines Board (IMB) will change its name to the Health Products Regulatory Authority (HPRA)....
- Monday, September 22, 2014
- 8:30am - 5:00pm
- York, United Kingdom
- Tuesday, September 23, 2014
- 8:30am - 5:00pm
- Manchester, UK, United Kingdom
- Tuesday, September 30, 2014
- 8:00am - 5:00pm
- Boston, Massachusetts, United States
- Thursday, October 2, 2014
- 10:00am - 11:00am
- NA, Massachusetts, United States