Manus Aktteva
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Manus Aktteva Biopharma LLP, An ISO 9001:2008 Certified organization, is a well informed, highly efficient and swiftly functioning competitive sourcing entity.
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- EDQM set to implement European Pharmacopoeia Version 6.8 in June 2010
European Directorate for the Quality of Medicines & HealthCare (EDQM) will
Manus Aktteva is an ISO 9001:2008 certified sourcing organization
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About Us

Manus Aktteva, the name suggestive of an "Active Hand” derived by the Latin word Manus meaning Hand and Aktteva being an ornamentalized version of Active. Manus Aktteva Biopharma LLP is an ISO 9001:2008 certified sourcing organization. 

Manus Aktteva Biopharma LLP is a well informed, highly efficient and swiftly functioning competitive sourcing entity.

Ability to synthesize newer API’s (Active Pharmaceutical Ingredients, Active Pharmaceutical Rawmaterials) and its advance intermediates; advance pharmaceutical intermediates in highly efficient network facilities in India, China etc where in very many projects have been successfully initiated to the buyers satisfaction and concluded along with submission of technical documentation as required for Drug Master File (DMF) filing.

Very many other projects for synthesizing API’s or synthesizing cumbersome intermediates and molecules are under progress in different stages from initial route scouting and synthesis to commercialization under the due supervision of Manus Aktteva.

Capability to support the buyer’s requirement of documentation and tech pack for evaluation prior to startup of project followed by preparation of documentary support as required by regulatory authorities.

Facilitating product synthesis by alternative and/or patent non infringing routes in many cases. 

Manus Aktteva Biopharma LLP has undertaken representations from manufacturers for selected territories or selected customers and/or selected products under long terms arrangements and agreements. Manus Aktteva Biopharma LLP is open for new representations for specialized products in specific territories or for specific customers. 

Manus Aktteva Biopharma LLP is an efficient exporter based in INDIA transferring the “ADVANTAGE INDIA” benefits. 

Actively interacting and fulfilling various Nutraceuticals requirements across the globe. 

We undertake to serve the industry in almost all spheres by facilitating the sourcing of required Pharmaceutical raw materials to various advance level intermediates and molecules in the field of Pharmaceuticals, Nutraceuticals, Specialty Chemicals and Biotechnology. We are serving major pharmaceutical companies to R&D facilities, small facilities to remotely placed facilities and institutions– efficiently and promptly across the globe. 

Manus Aktteva Biopharma LLP has associated with MNC’S, Pharma majors and of course medium sized and small formulation companies. The satisfaction and appreciation from both buyers and the supplier’s level has been over whelming and this is the main driving force for better performance in future. 

Our goal is to achieve the fastest possible result for the person/institution in search of API’s or its advance level intermediates in the pharmaceutical sector - whether the requirement is related to the simplest to the most complex hard to find new and upcoming molecules and be COMPETITIVE AS WELL. Due to fastest interaction and feedback of the accurate data and identification of the most competitive suppliers, mega Pharma companies to the smallest formulators are using our services.

  • Manus Aktteva Biopharma LLP, India is successfully representing suppliers, manufacturers from INDIA, suppliers, manufacturers from CHINA, and fulfilling the requirements of buyers from EUROPE, USA, South America, Japan, Korea, Taiwan, Australia, & middle-east.
       Keywords: New Molecules, patents, R&D, cas, cas number, product, supplier, suppliers, vendor, vendors, price, prices, api, apis, active pharmaceutical ingredient, ingredients, importer, exporter, distributor, import, export, sale, producer, manufacturer, synthesizer, synthesis, gmp, cgmp, fda, dmf, cgmp, cos, inventory, stock, prompt shipment, compounding, compound, research, development, patent, r and d, pharma
  • Please note that products falling in to controlled substance category shall be exported directly from the manufacturer principals only against receipt of original import permission issued by concerned authorities of the importing country.
  • => Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
        => Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1)
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