
Farmavita.Net member is developing innovative concept for glogal branding and distribution of remedies and devices for therapy of arthritis.
Company is looking to joint-venture, collaborative development or in-licensing of non-prescrition products, on exclusive basis.
For more details please contact Farmavita.Net.

Farmavita has developed Renarthro, the synergistic combination of frankincense and myrrh extracts, with Osteol. Renarthro is formulated to quickly alleviate pain, decrease inflammations and preserve joint health.
Hi,
We are a Pharmaceutical company, based in Casablanca Morocco, specialized on dermatology.
We are looking for dossiers (european or CTD) of topical products or liquid (generics products with down payment or local manifacturing under license)
Sincerly.
Issam
The EU CTD dossier is in development.
Farmavita.Net member is looking for OTC medicatios against vaginal infections. Product should be approved in EU and have up-to-date CTD Dossier. Licensee will also close exclusive supply agreement with licensor.
Examples of suitable products are monoproducts or combinations of fluconazole, itraconacole, clindamycine pessaries and cream, as well as smiilar products.
Dear Members,
We require technology to manufacture Sirolimus and Daptomycin. Companies / Individuals who can provide the strain and knowhow can contact us stilbenebio@yahoo.com
Thanks and regards
Prasad
The gradual spread of software automation in drug development may be
getting a boost from open source systems. Most e-clinical systems
today--from data capture and storage to trial management and
operations--are proprietary, despite the excellent work that solutions
providers have done to make their products compatible with existing
standards-based and de facto standard industry systems.

Approval of the drug product for import, manufacturing and marketing in India, its demonstration for safety and efficacy in humans is essential. The Rules 122A, 122B and 122D, 122 DA, 122DAA, 122E and Appendix I, IA and VI of Schedule Y of the Drugs & Cosmetics Act, 1945, describes the information/data required for approval of clinical trial and/or to import, manufacture, or market any new drug in the country. However, the requirements for approval of clinical trials and new drugs may vary depending on the nature of new drugs.
The whole 11 pages article is available for download at Downloads section of Farmavita.Net.
Budapest, June 21-22, 2012
What do you do when the EMA or the FDA comes knocking? Are you absolutely confident that everyone is fully prepared? Every clinical trial is subject to audits as well as health authority inspections from time to time, verifying compliance with rigorous requirements that have in fact changed significantly over the last few years. In this masterclass you will learn, develop and practice what you need, to be ready when the call comes, taking you through from the announcement to the end of the process.
Datamonitor's industry profiles are an essential resource for top-level data and analysis. This profile includes data on market size and segmentation, plus textual analysis of the key trends and competitive landscape, demographic information, and descriptions of the leading companies.
Jobline - Job opportunities published at Farmavita.NetAt the JobLine you can post your job vacancies or search for new job opportunities. We kindly invite all members to post their demand for full-time/part-time jobs, temporary needs, consulting support, project support, internship openings and other opportunities. If you are recruiter or just looking for job ..... find below important presentation which will describe you why are social networks are important to your career. |
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