Manus Aktteva
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Manus Aktteva, confidentiality agreements, sourcing, molecule, research services, customized technical package, evaluation, non infringing routes, synthetic routes, expert consultation, properties, development, route scouting, process optimization
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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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Our Advantage

• Manus Aktteva Biopharma LLP undertakes all tasks with strict confidentiality and performs under confidentiality agreements put in place wherever required.

• Manus Aktteva Biopharma LLP is well informed efficient, prompt & competitive.

• Manus Aktteva Biopharma LLP takes up the projects with all the passion and zeal, may it be sourcing a molecule or carrying out and organizing the research services.

• Able to provide customized technical package with evaluation quantities in most cases.

• Ability to arrange supply of products with non infringing routes and can work with your process, or arrange to develop a new process; process development to simplify and improve difficult or expensive synthetic routes in very many cases.

• Available expert consultation facilities to trouble shoot for customers. Our experts painstakingly follow every step while searching for lead molecules and their properties. Our expertise lies in the development of process related parameters such as route scouting, process optimization, product isolation, product purification and scale up with the flexibility to refine our experimental protocols

• Documentation support in product synthesis when the buyers purchase of specific target intermediates is for filing Drug master file with regulatory authorities.

• Able to transfer “Advantage India “benefits smoothly.

• Ability to organize synthesis of most sought after molecules or even current molecules swiftly with final product/ intermediates & molecules well characterized, characterization done using our networked well equipped RND and analytical facilities with support of NMR, HPLC, LC-MS and the like.

• FTE service is always available at a very reasonable cost. Typically, a team led by experienced Ph.D. Chemists will be assigned to the clients special requirements. Weekly reports and tele-conference are regularly used for communication of project progress.

• Our innovative approach to tackle process development or to trouble shoot the problems helps our customers to succeed.

• "THE MANUS AKTTEVA BIOPHARMA LLP Team WILL CONSISTENTLY DELIVER SWIFT, VALUE BASED AND SATISFACTORY SERVICE TO ALL OUR CUSTOMERS", and this demonstrates our commitment to making your request an experience that could only be summed up by the words: "Test us to get the best of us".


  • 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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