About Assurgen

Bringing the high-quality, cost-effective products modern-day healthcare delivery.

Assurgen pharma strongly believes that with its expertise and innovation pharmaceutical business background, it is aptly positioned for APIs & Intermediates manufacturing and outsourcing for global market. We also undertake custom synthesis and contract manufacturing.

Established under Indian Companies Act 1956 vide CIN: U24232AP2013PTC090442 dated 10-10-2013 with its head office in Visakhapatnam, Andhra Pradesh.

Never content to rest on our laurels, Assurgen Pharma has set our sights on being best in the nation. Our name itself (assurance "Assur") reflects a commitment to being quality of a product and its spelling ("gen" at the end, instead of "generic") recognizes our product chemical makeup and finally “Pharma” a product to be marketed under its brand name to the customers.

Our multiple cGMP-manufacturing facility and world class R&D center is located in the heart of vizag APSEZ De-modified area with well connected to road, rail and air enabling cargo movement to the nearest transport facility.

To be widely recognized in the global market as a valued leader and successful cGMP compliant resource in developing and trading manufacturers of active pharmaceutical ingredients and intermediates.

Work as hard and as best as you can. We take a progressive approach to become the most admired, trusted and innovative brand in the global market.

Our core values determine our strength, behaviour and every interaction with customers. We give more priority to care, leadership and customer proximity than business success. Our values reflect our responsibility towards better future.

Our main quality policy is to achieve the highest possible customer satisfaction.

We take priority on manufacturing drugs with highest GMP standards.

  • High intensity
  • High efficacy
  • High safety
  • High quality
  • High purity
  • High flexible

Our products are manufactured and controlled according to cGMP rules. Details of manufacturing, as well as in-process and quality control, are documented and controlled.

New products are developed adhering to the GMP and GLP guidelines applicable to research and development.