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General Info |
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Latest News |
- EDQM set to implement European Pharmacopoeia Version 6.8 in June 2010 European Directorate for the Quality of Medicines & HealthCare (EDQM) will
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Supplier Registration Form |
F/Pur/03A/Issue No.01 |
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An online supplier registration form has been made available for prospective suppliers to submit their registration requests to Manus Aktteva. Only suppliers/manufacturers seeking to do business with Manus Aktteva and who are currently not the approved suppliers for Manus Aktteva Biopharma LLP should submit their details using the online form. Please fill out the below form completely. You will be contacted by one of our representatives shortly regarding your product. By becoming a part of the database, your company’s information will be available to our procurement personnel when sourcing activity occurs.
All information is considered confidential and will not be disclosed or sold to anyone.
- Mandatory fields are marked with asterisks (*). Registration form cannot be submitted without filling up the mandatory fields.
- Information on the online registration form will be lost if the window is closed without submission and receiving the registration confirmation on the next page.
- Any additional documents required for the registration should be attached in the Attachments section.
- Registration is only a process for your showing interest in doing business with us and does not guarantee for business from Manus Aktteva. Based on the requirement of similar products as per profile, we will get in touch with you.
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NOTE:
- 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.
PATENTS:
- => 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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Queries |
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Tel1: +91 79 65123395 |
Tel2: +91 79 26463395 |
Email: click here |
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