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Equipment Logbooks: Good Practices and Regulatory Requirements

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₹199
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Overview of GMP and Quality Concepts in Pharmaceuticals and Biotechnology

Ameena

Free
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An Interactive Guide to Good Documentation Practice

Ameena

Free
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Personnel Qualification and Training in GxP Environments

Ameena

Free
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An Interactive Guide to Good Documentation Practice

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Free
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Maintaining Data Integrity in GMP Environments

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Free
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Personal Hygiene in GMP Environments

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Free
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Handling Product Complaints and Recall

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Free
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Understanding the "Why" and "How" of GMP Audits

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Free
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Aseptic Processes and Cleanroom Basics

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Free
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Personnel Qualification and Training in GxP Environments

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Free
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Compliance Monitoring Procedures for Good Laboratory Practice : OECD 2

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Free
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Conduct of Laboratory Inspections and Study Audit : OECD 3

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Free
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Compliance of Laboratory Suppliers with GLP Principles : OECD 5

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Free
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Application of the GLP Principles to Field Studies : OECD 6

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Free
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Application of the GLP Principles to Short Term Studies : OECD 7

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Free
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Role and Responsibilities of the Study Director in GLP Studies : OECD 8

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Free
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Preparation of GLP Inspection Reports : OECD 9

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Free
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The Role and Responsibility of the Sponsor in GLP Studies: OECD 11

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Free
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Requesting & Carrying Out Inspections /Study Audits in Another Country : OECD 12

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Free
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Application of the Principles of GLP to in vitro Studies : OECD 14

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Free
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Guidance on the GLP Requirements for Peer Review of Histopathology : OECD 16

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Free
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Application of GLP Principles to Computerised Systems : OECD 17

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Free
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Relationship between the OECD Principles of GLP and ISO/IEC 17025 : OECD 18

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Free
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Management, Characterisation and Use of Test Items: OECD 19

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Free
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Guidance for Review of the GLP Status of Non-Clinical Safety Studies : OECD 20

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Free
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Possible Influence of Sponsors on Conclusions of GLP Studies : OECD 21

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Free
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GLP Data Integrity : OECD 22

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Free
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Quality Assurance and GLP : OECD 23

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Free
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Quality Improvement Tools and GLP : OECD 24

Ameena

Free