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India
combines many opportunities and many challenges for the pharmaceutical
industry. This webcast CD provides an overview
of product registration as well as regulatory requirements
for importing, manufacturing, or selling drugs in India.
GMP, QA/QC, and labelling requirements will also be discussed.
This Indian presentation has 78 PowerPoint slides.
Click
here to see a sample
page of our webcast presentation.
The following topics are covered in this webcast:
- Country overview
- Health care system
- Pharmaceutical industry overview
- Pharmaceutical regulations
- Administrative structure for pharmaceuticals
- Health insurance and reimbursement
- Prescription versus generic products
- Recent and proposed changes in pharmaceutical
policy
- Import registrations, import licenses
- Manufacturing licenses
- GMP
- QC and QA
- Sale licenses
- Packaging and labeling
- Product
standards
- New drug approvals
- Clinical trials
- GCP
- GLP
- Price controls
- Intellectual property rights
This webcast
is designed for pharmaceutical professionals in regulatory
affairs, business development, international sales
and marketing, or anyone who wants to be current on
a number of Indian regulatory and business
issues.
Our
speaker is Mr. Patel,
PBM's partner in India.
He has
twenty years of experience in Indian regulatory affairs.
Click here to purchase a CD which includes
the audio and PowerPoint presentation.
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