Welcome to
Vineet Analytical
Vineet analytical is work with more than expectation to quality for cGMP and GPL for organic compounds, active ingredients and formulations used in pharmaceutical health care society, we work for pharmaceutical manufacturer’s, research and development (R&D) licenses as the contract analytical testing site.
We carried out collaboration research work and we allow customer audits and audits by foreign regulatory bodies. After successfully formulation of the drug and it has been approved the reports from the clinical trials department are forwarded to be approved by the regulatory body for pharmaceuticals and medical advices at FDA, USFDA and the central drugs standard control organization (CDSCO) in India.
After the approval, further inspections are performed to check the drug are forwarded for further research.
More about us
We carried out collaboration research work and we allow customer audits and audits by foreign regulatory bodies. After successfully formulation of the drug and it has been approved the reports from the clinical trials department are forwarded to be approved by the regulatory body for pharmaceuticals and medical advices at FDA, USFDA and the central drugs standard control organization (CDSCO) in India. After the approval, further inspections are performed to check the drug are forwarded for further research.
1. Thesis writing
2. Research paper writing
3. Plagiarism report
4. Schrodinger report
5. SciFinder report
6. Molecular modeling and docking
7. Patent drafting and Copy write filling
8. Patent Examination
9. Research proposal writing
10. Interpretation of IR, NMR, Mass etc.
AR grade
LR grade