PRE-SCREENING

Pre-screening of Regulatory documents of production , quality assurance , quality control, clinical trial and Pharmacovigilence department are extremely important to avoid multiple queries and warning from NRA , USFDA and other International Regulatory Agencies.
Pharmaguide introduces in process check of documentation, audit and conduct of training of company professionals in their facility and guides the regulatory departments for validation process.
Our experts having pioneered in GMP / CGMP/ WHO Pre-qualification Audit will guide and draw a regulatory pathway for Validation.

For Free Consultation Contact 7661077363 or mail to info@pharmaguideservices.in, mailtrack149@gmail.com