Certificate Program in Good Laboratory Practice | Enhance Your Lab Skills | Cliniminds

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Good Laboratory Practice

pharmaceutical business analytics distance course

Distance Learning

✔ ACCRE USA Accredited
✔ Program developed by senior industry experts
✔ eBooks – Presentation & Notes on Cliniminds LMS
✔ Cliniminds Certification after completion of program
✔ MCQ based final exams
✔ Introduction to GLP | Fundamentals of GLP | OECD GLP principal | WHO GLP in brief | GLP Lab Set Up | SOP | DQ, IQ, OQ, and PQ | facilities | instrumentations and software | Personal selection | Staffing and training | Quality control procedures | QA | Documentation and Archiving | Gap analysis | Analysis of Samples and QA | Chromatography review | Integration parameters | Quality assurance Reporting and Investigation of Experiments | Complete experimental work from start till end | Study objective | Description of test system | Results and discussion | References | GLP complaint statement | QA statement | Investigations - Study based, Facility based, and process-based Data Storage and Retrieval and Maintenance of Archive | Records to be archived | Indexing | Placing the records | Document transfer | Retention period | Disposal | Dedicated electronic archiving system and maintenance Introduction to GDP | Standards of GDP and its purpose | Typical element of documentation | Common documentation error GCLP audit and Inspection | Element of GCLP inspection | Inspection objective | Types of inspection and its application to 21 CFR part 320 and method validation | Conducting a GCLP inspection of a BE study | Inspection of analytical data | Problem areas of GCLP inspection

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Good Laboratory Practice Course Details

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