Training

Transformation with Training

Blue Ocean strongly believes that evolution of personnel has a major role in the success of any organization. And Blue Ocean imparts effective training applying the elements which has a deep impact on the thought process of personnel. Hence there is a high probability that it will bring transformation on your site.

Under this era following types of training are imparted. Based on the subject they may be classroom/on-job training.

Hybrid Training

Which is a combination of Audit & Training

Training the Personnel (Officers & above)

On CGMP Topics as mentioned below as per the regulatory requirement

Training programmes for Blue-Collar Employees

On cGMP as per the regulatory requirement in Indian local languages Hindi, Marathi and Gujarati apart from English

Training Topics for Industry

  • Training Sessions of "Blue Ocean of Compliance" on your site covering all the Topics in the book
  • Transforming workshops on the book "Blue Ocean of Compliance" to discuss the contents of the book
  • Implementation of the book "Blue Ocean of Compliance" on your site
  • Data Integrity
  • ICH 07
  • CGMP 21CFR211 & 210
  • Good Documentation Practices (GDP)
  • Good Laboratory Practices (GLP)
  • How to face Regulatory Audits successfully
  • Regulatory Submission an overview of the US & EU market
  • Risk Assessment
  • Equipment Qualification
  • Out of Specification & Investigations
  • Investigations
  • Deviation, Change Control, CAPA (Quality Management Systems)
  • How to do Internal Audits effectively to be ready to be inspected anytime
  • Body Language while facing the Regulatory Audits
  • Dos and Don't in Regulatory Inspections
  • Special Training for blue-collar employees
  • Other Topics may be based on the request

Training Topics for Pharmacy & Science Colleges

  • Lectures on "Blue Ocean of Compliance" Book to explain the concept of Regulatory Inspections Audit & Compliance & Quality Culture
  • Career/Growth Opportunities in Pharmaceutical Industry
  • Functions of different departments of the Pharma Industry QA, QC, Warehouse, Production, Engineering
  • Data Integrity
  • ICH Q7
  • CGMP 21CFR211 & 210
  • Good Documentation Practices (GDP)
  • Good Laboratory Practices (GLP)
  • Other Topics may be based on request