Crambridge | All Courses

All GMP QC, QA and Regulatory

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

Cultivating Diversity, Inclusion, and Belonging at Work

Conflict of Interest Management

How to Conduct an Effective Job Interview

Employee Health and Wellness

Client confidentiality

Biosimilarity II: Development and Approval

Self help guide to managing Covid - part 1

Self help guide to managing Covid - part 2

Quality Guidelines for Pharmaceutical Development ICH Q8

ICHQ7

Basic Electrical Safety at Home and Offices

Personal protective equipment(PPE)

HVAC validation

Electrical essentials

Equipment Logbooks: Good Practices and Regulatory Requirements

Overview of GMP and Quality Concepts in Pharmaceuticals and Biotechnology

An Interactive Guide to Good Documentation Practice

Personnel Qualification and Training in GxP Environments

Maintaining Data Integrity in GMP Environments

Personal Hygiene in GMP Environments

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

Aseptic Processes and Cleanroom Basics

Personnel Qualification and Training in GxP Environments

Compliance Monitoring Procedures for Good Laboratory Practice : OECD 2

Conduct of Laboratory Inspections and Study Audit : OECD 3

Compliance of Laboratory Suppliers with GLP Principles : OECD 5

Application of the GLP Principles to Field Studies : OECD 6

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

Preparation of GLP Inspection Reports : OECD 9