QUALITY

At Neogen we endeavour to supply consistent quality product and surpass customer expectations.

All the sites have independent facilities for quality checks and safety. The manufacturing facilities have following accreditations:

Mahape Facility– ISO 9001:2015 from Bureau Veritas Certification Holding SAS
Vadodara Facility– ISO 9001:2015, ISO 14001:2015 and ISO 45001: 2018 certifications from Bureau Veritas Certification Holding SAS
Dahej Facility– ISO 9001:2015, ISO 14001:2015 & ISO 45001:2018 Certified by Bureau Veritas Certification Holding SAS and GMP Certified By SGS
Hyderabad Facility– ISO 9001:2015, ISO 14001:2015 & ISO 45001:2018 Certified by Bureau Veritas Certification Holding SAS and GMP Certified By SGS
Implemented current good manufacturing practice (cGMP) prescribed by the US FDA as applicable for intermediates

Our documentation system is also as per ICH-Q7A guidelines as applied to intermediates.

At Neogen, we have an independent quality assurance (QA) and Quality Control (QC) team of 57 member, which reports directly to the top management and is responsible for documentation and data control. The team is also responsible for the release of batches for sale. The QA team organizes frequent internal and external audits.

All of our sites have been validated and audited by multiple customers from the pharmaceutical industry in India, Europe and Japan. We have also been audited by several large agrochemical companies from all over the world.

Our Quality Control laboratories work round the clock and are adequately equipped with analytical equipment like GC, HPLC, UV Spectrophotometer, Karl fischer Moisture Analysers, Polarimeter, Inductive Coupled Plasma (ICP) etc.

Analytical equipment is also added as per specific customer needs.