Quality Policy

We, at Manus Aktteva Biopharma LLP commit ourselves for supplying products that would give complete satisfaction to our customers.

We will strive to achieve growth and leading position in the market by:
  • Supplying quality products as per our customer’s necessary and essential requirements, meeting Domestic & International standards (complying with the requirements of Regulatory & Non-Regulatory markets) of quality, performance and reliability.
  • Complying statutory & regulatory requirements and continually improving the effectiveness of Quality Management Systems.
  • Creating an environment of team work and innovative approach.

MANAGEMENT
1ST SEPTEMBER 2017

ISO 9001:2015 Certification

Manus Aktteva Biopharma LLP is certified with ISO 9001:2015 certification.

ISO 9001:2015 Certificate
pharmaceutical intermediates
MSME Registration
pharmaceutical intermediates


Why Us
Your product search made swift, simplified & successful in experienced hands. Test us to get the best of us Active Pharmaceutical Ingredients & Intermediates. New Molecule R&D, Scale up & Commercialization Technical Data package, CMC data package & Drug master files for most of the products as a part of our service Our partnerships are market-driven and are aimed at delivering real business value to our clients To Strive harder & excel further for the sevice of mankind by offering our services to the industry

Global Sourcing

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