GAP Analysis Audits are conducted by us greatly to support the clients in Facility Compliance. We analysis is a way to compare current conditions and practices in order to identify gaps and areas in need of improvement with regards to compliance with the relevant standards, defined by Health Authorities. Based on the outcome of GAP Analysis Audit and Extension of Support by deputing ours team at Site during authority inspection and Support in Post-inspection CAPA Closure for submission to the authority The guidance provided by us also includes extensive training to the staff in maintaining Compliance and going through inspections. In this way, MEDATEQ LABS helps to clients that compliance with the relevant standards to Health Authorities. MEDATEQ LABS providing services such as GAP analysis in pharmaceuticals, GAP assessment in the pharmaceutical industry, GAP analysis and facility assessment, and GAP assessment in pharma industry.

MEDATEQ LABS one of the leading pharmaceutical GMP audit consulting firm in India. We help to the pharma industries to identify all the Gaps and also help to find which process need to be fixed like quality management process, internal communications process, document control process, record keeping process, training process, internal audit process, management review process, measuring and monitoring process, nonconformance management process, and continual improvement process.

GAP analysis in pharmaceutical industry
GAP Analysis and Facility Assessment
Gap Analysis/Regulatory Assessment
Optimizing Operational and Quality Systems
Data Integrity and Management Challenges

Regulatory Assessment
ISO 13485
ISO 22716 for Cosmetic Ingredients
ISO 15378, PS 9000 For Primary packaging for medicinal products
US 21 CFR 210-211 (cGMP)
EU IPEC GMP
EU IPEC GDP for Pharmaceutical Excipients
EU GDP for API
EU GMP part II for API (ICH Q7)
US 21CFR 820