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GUIDELINES FOR GOOD PRACTICE IN THE CONDUCT OF CLINICAL TRIAL... Page 1 of 72 GUIDELINES FOR GOOD PRACTICE IN THE CONDUCT OF CLINICAL TRIALS IN HUMAN PARTICIPANTS IN SOUTH AFRICA Back to DOH Policy
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What is guidelines for good practice?
Guidelines for good practice are a set of established standards and recommendations that outline the best practices and procedures to follow in a particular field or industry.
Who is required to file guidelines for good practice?
The individuals or organizations responsible for implementing the guidelines are typically required to file them.
How to fill out guidelines for good practice?
Guidelines for good practice can be filled out by carefully following the provided template or form, ensuring that all required information is included and accurately documented.
What is the purpose of guidelines for good practice?
The purpose of guidelines for good practice is to provide a framework for achieving optimal performance, safety, efficiency, and compliance within a specific field or industry.
What information must be reported on guidelines for good practice?
The specific information that must be reported on guidelines for good practice may vary depending on the industry or field, but it generally includes details about the recommended procedures, standards, protocols, and any necessary documentation or evidence.
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