I am searching for information for the regulation of Intra Ocular lenses and Autoinjectors in India and S. Korea.
Are there specific regulations or guidelines that must be followed to register these products in both India and S. Korea?
How long will a product approval take for a re-registered product that includes a manufacturing site change?
Thank you.
Yvonne
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Yvonne Middlefell
Executive Director Regulatory Affairs
NSF Health Sciences
Culbokie
United Kingdom
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