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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?
*
Yes
No
Does the manufacturer have a valid GMP certificate issued according to the national requirements of an EAEU member state or EAEU requirements?
*
Yes
No
Has the application for GMP inspection already been submitted to the authorized body?
*
Yes
No
What support do you need?
*
Preparation of the site for inspection with a preliminary audit
Preparation of the site for inspection without an audit (sending a checklist, list of typical observations, teleconference with the site (Q&A session)
Response to the authorized body's and/or inspectors' request before the inspection
Accompanying the inspectorate during the site visit
Support in preparing a corrective and preventive action plan (CAPA) based on inspection results
Other
Additional conditions and requests
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Your name
*
Email
*
Phone number
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