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M/s Skymax Research & Regulations

About Us

Skymax, a truly research base organization believes in constant development of excellence in the field of research and development as per the need of the Pharma industries. We are into contract Research & Development and Regulations management to cater the Research & Regulatory need of the pharmaceutical industries globally.
Looking to the scenario of highly regulated pharmaceutical industries, Skymax has created his own network to serve the Research & Regulatory need of the pharmaceutical industries.
Skymax is tied up technically with reputed approved Research centre and CRO’s which can provide perfect clinical solutions. Our Associates analytical laboratories are of GLP standards and able to provide accurate analytical solutions. And our associate overseas consulting agencies guide us in concern with the day to day updation in the sector of Research & Regulation, act to serve better to our domestic and overseas clientle.

Our core regulatory team will validate, prepare, reform and arrange the technical data in an order to the country specific format for the fastest regulatory approval


Skymax, a truly research base organization believes in constant development of excellence in the field of research and development as per the need of the Pharma industries. We are into contract Research & Development and Regulations management to cater the Research & Regulatory need of the pharmaceutical industries globally.
Looking to the scenario of highly regulated pharmaceutical industries, Skymax has created his own network to serve the Research & Regulatory need of the pharmaceutical industries.
Skymax is tied up technically with reputed approved Research centre and CRO’s which can provide perfect clinical solutions. Our Associates analytical laboratories are of GLP standards and able to provide accurate analytical solutions. And our associate overseas consulting agencies guide us in concern with the day to day updation in the sector of Research & Regulation, act to serve better to our domestic and overseas clientle.

Our core regulatory team will validate, prepare, reform and arrange the technical data in an order to the country specific format for the fastest regulatory approval


Clinical:
Skymax has created his own associate network with different CRO’s, which is certified by the Govt .Regulatory authority. In our associate network we are having approved CRO’s of European Union, UK, USA, Brazil, and more to meet the international standards of various types of clinical studies. The most efficient way to conduct and control clinical trials is to make the best possible use of statistical methodology in their design and analysis, and of advanced technology in their conduct. Our Clinical Data Management service has years of experience in providing a full range of data management services for the pharmaceutical, biotechnology and medical device industries, across many therapeutic areas. We have the experience, capacity and technological innovation to meet today's pressures in speeding processes to database lock while retaining high quality deliverables.

Analytical:
We are having our in house well equipped , and well documented analytical laboratory to manage analytical solutions of our client , and Our Associate Laboratories are recognize by various Govt. Regulatory Authority and also of GLP standards to meet the international analytical standard.

Process:
We are having our own in house Formulation & Development department for development of various process validations, Pivotal batches, pilot trials, and commercial production and its documentations up to technology transfer to meet the requirement of our client.

Regulatory: Our in house core regulatory team is keenly monitored the studies, methods, and processes. They validate, rectify, approve and arrange the technical data in an order to the country specific format for the fastest regulatory approval.
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