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Questionnaire for preparing a commercial proposal for GMP audit/inspection

Your company name

In which country is the manufacturing site located?

Which pharmaceutical substances are planned for audit/inspection at this manufacturing site?

Will sterile pharmaceutical substances be produced at the site?

Does the manufacturer have a valid GMP certificate issued according to the national requirements of an EAEU member state or EAEU requirements?

Has the application for GMP inspection already been submitted to the authorized body?

What support do you need?

Additional conditions and requests

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