A> Good Pharma Practices Training Modules (GPP)

GPP1>> Process Analytical Technologies (PAT) & Corrective Prevention Action Program (CAPA)
GPP2>> Risk Based GMP Audit
GPP3>> Advances in Pharmaceutical Science
GPP4>> Project Management in Pharmaceutical and Bio Technology
GPP5>> Compliance with cGMP & GMP Requirements
GPP6>> International GMPs: Compliance requirements with US, EU and Japan
GPP7>> Programmes on Validation: Cleaning,Process & Formulation Equipments, API & Formulation Process
GPP8>> Deviation Reporting System

B> Quality Assurance & Audit Training Modules (QAA)

QAA1>> Pharmaceutical Laboratory Control for FDA Compliance and Test Method Validation
QAA2>> Advanced Topics in Clinical Research and Drug Development
QAA3>> Drug Safety Surveillance & Epidemiology
QAA4>> Methods Development, Validation Procedures and Conformity Assessment in the Analytical Laboratory
QAA5>> Quality Assurance and Audit Requirements in Hospital Based Clinical Trials
QAA6>> Qualification and Validation of Lab Systems and Validation in the Pharmaceutical Laboratory (IQ, OQ, PQ)
QAA7>> Regulatory requirements & guidelines for Clinical trials

C> Safety & Risk Management Training Modules (SRM)

SRM1>> Design Control, Software Validation, & Safety Risk Management

D> Marketing & Product Development Training Modules (MPD)

MPD1>> Product Management
MPD2>> Consultative Marketing Skills Development
MPD3>> Good Distribution Practices (GDP)

E> Pharmaceutical Resource Building (PRB)

PRB1>> The Qualified Person (QP): Relevance, Role and Responsibilities and Requirements in the Regulated Industry Systems
PRB2>> The Qualified Person (QP): Relevance, Role and Responsibilities and Requirements in the Regulated Quality Systems