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Pharmaceutical Validation Training

Pharmaceutical Validation Courses

About Course

Validation plays a Key Role in Pharmaceutical , Clinical Trial , Medical Device , Food, Biological industries. Validation helps one establish and demonstrate that a particular activity is maintainig a desired level of compliance.

  • Pharmaceutical Valiadtions Courses is desgined for individuals who need basic, but thorough understanding of all the validation in pharmaceutical industry.
  • It will help to understand the fundamentals and concepts of Pharmaceutical Validation.
  • Overview and understanding of Pharmaceutical validaion, how to organize and carry out the same & the Key areas to Look forward in the whole process
validation-training

Scope

  • To Study the Basic Fundamentals of Pharmaceutical Validation
  • To Understand the importance and underlying principles of pharmaceutical Validations
  • To Create a thorough/increase understanding of :
    • Validation
    • Process Validations
    • Analytical Validation
    • Equipment Validation
    • Validation Master Plan
    • Cleaning Validation
    • IQ/OQ/PQ,Commissioning Activites
    • Computer System Validation
  • Our Industry experts have developed the modules in such a way that it gives the participants in-depth knwoledge of the above mentioned points in Validation

Learning Outcome

  • Understand Regulatory Concepts
  • Able to write and review Regulatory Documents
  • Marketing Authorization from different countries
  • Become an RA professional
  • Preparation for audits and inspections
  • Advance to an higher level in RA career ladder

Who Should Apply

  • This course is ideal for anyone in the Pharmaceutical, Medical Device, Biotech, Biopharmaceutical and Skin/Cosmetic industries who is tasked with validation activities
  • Documentation Department
  • People involved in validation activities from product development to post-approval production concerns will find a complete insight on what regulators are looking for.
  • Research Chemist, Quality Control Chemist, CRO's, Productions,RA etc involved in Documentation
  • Will be beneficial to personnel directly involved in process/product development, manufacturing, quality control/assurance departments
  • Beginners will get to understand the in & out of Pharma Validation and Experienced Professionals can look forward to update their existing knowledge

Eligibility

Graduates in any stream of science are eligible to apply.

Duration & Fees

  • Course Duration : 3 Months
  • Fees: Rs 11,500-/

Apply Online

Students can download the admission form by clicking here, in PDF format print and fill the same, clearly mentioning Mobile No & Course Interested.The Filled form should be courried to us along with DD at the below mentioned address.

Address:
Global Institute of Regulatory Affairs
Prestige Classic BLD,
D Wing Off G4 & 5,
Chinchwad Station,
Near Dawabazar,
Chinchwad Pune - 19
Phone – 020-46704472

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Testimonials

    Nakul Pathak Says

    "Regulatory Affairs program at GIRA very effectively integrates industrial experiences with academics in the pharmaceutical field. It helps you to understand the Practicalities of the rules, regulations & guidelines ."

    Nikhil Pachpute Says

    “GIRA's training institute offers high quality courses. It gave me a much needed broader perspective and a multi- faceted view of regulatory affairs. I understood the department work in depth and got a breakthrough in Regulatory Sector."

    Arun Renukuntla Says

    "Faculty at GIRA has vast industrial experience, which has been very useful for me. The teaching methodology is very innovative as well as interactive. Dedicated sessions for query solving are also there.”

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