- Good documentation makes up a necessary part of the quality assurance system. Written policy prevents errors resulting from spoken communication, and clear documentation authorize tracing of activities performed.
- form must be designed, prepared, reviewed, and distributed with care.
- Documents must be approved, signed, and dated by the suitable competent and authorized persons.
- Documents must have distinct contents. The title, nature, and purpose should be distinctly stated. They must be laid out in a well-ordered fashion and be easy to check the reproduced documents must be clear and legible.
- Documents must be regularly reviewed and kept updated. When a document has been revised, systems must be operated to prevent accidental use of superseded documents (Example only current documentation should be accessible for use).
- Documents must not be handwritten; however, documents require the entry of data, these entries may be made in understandable legible handwriting using a suitable indelible medium (i.e., not a pencil). Enough space must be provided for such entries.
- Many shortcuts may create a risk that can be expensive in the end.
- Each step in a procedure has been covered for a purpose.
- Manufacturing Companies
- Pharmaceuticals Companies
- Food Manufacturing Companies.
How to get GMP Consulting Services in Norway?Certvalue is providing GMP Consulting Services in Norway with extensive expertise and experience in all International food and pharmaceutical products Standards. For GMP Certification in your organization, reach Certvalue – GMP Consultants us at +776017362326 Send your requirements to Our experts will call you and guide for Successful GMP Certification in Norway. We would be happy to assist your company in the GMP Certification process in Norway to send your research after contact @certvalue.com.
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