Pharma Tips

Post Graduate Diploma in Drug Regulatory Affairs

By: Pharma Tips | Views: 6730 | Date: 26-Feb-2013

Good option for working professionals due to weekend/Sunday batchesExperienced industrial faculties to deliver lectures and solve the queriesKnowledge can be applied on-jobHelp students strengthen their professional & soft skillsShort term courses(3-6 Months) give a competitive edge when it comes to job promotionsWeekly news updates about pharma regulations

Greetings from Institute of Pharmaceutical Management!!


Admissions started for Post Graduate Diploma in Drug Regulatory Affairs’ 

 

Branch

Batch No.

Commencement date

Vashi

6th Batch

10th March 2013

Borivali

10th Batch

2nd June 2013

Dombivli

16th Batch

16th June 2013

 

 Upcoming courses commencing in March 2013:-

@  Diploma in Pharma Production Management

@  Diploma in Pharma Quality Control management

@  Diploma  in Pharma Quality Assurance management

@  Diploma in Pharma Purchasing, Warehouse & Inventory management

@  Diploma in Pharma Packaging management

@  PG Diploma in Pharma GMP

 

Benefits received by students:

@  Good option for working professionals due to weekend/Sunday batches

@  Experienced industrial faculties to deliver lectures and solve the queries

@  Knowledge can be applied on-job

@  Help students strengthen their professional & soft skills

@  Short term courses(3-6 Months) give a competitive edge when it comes to job promotions

@  Weekly news updates about pharma regulations

 

About IPM:

@ Institute of Pharmaceutical Management, a pioneering institution for Pharmaceutical training in India led by Ms Anagha Maharao, Director having 26years of experience in pharma industry.  It conducts courses in Regulatory Affairs,GMP & Patent Laws.

@ Ms. Anagha Maharao – Principal trainer and favourite tutor among IPM students. Her valuable experience and teaching expertise coupled with affable and terse communication skills puts students at ease and increases their thirst for knowledge.

 

Achievements:

@5 years of excellence in imparting knowledge

@Branches in Dombivli,Borivli and  Vashi

@More than 1500 enrollments

@ International enrollments from Spain, New York, UK, Vietnam,Oman and Johannesburg

@Students are getting jobs as per their desired profile

@Classroom and Distance participation courses available

 

Post-graduate Diploma in Drug Regulatory Affairs - Syllabus highlights:

@  Introduction to Pharmaceutical Quality System

@  Introduction to various Regulatory agencies – CDSCO,EMA,EDQM, USFDA, MHLW, WHO

@  ICH Quality guidelines - Q1,Q2,Q3, Q6

@  ICH Q M4 CTD format

@  GMP overview, Change control, GMP inspection

@  DMF preparation in CTD format

@  Regulatory Submission to US

@  Regulatory submission to Europe 

@  Regulatory submissions to Other agencies-WHO, Canada and Japan

@  Handling deficiencies w.r.t. above submissions

@  Dossier preparation in CTD format

@  Regulatory Systems in US, ANDA submissions, handling post approval changes

@  Regulatory Systems in Europe, filing procedures, handling variations

@  Drug Registration with Latin America

@  Handling deficiencies from Drug Regulatory Authorities w.r.t. above submissions

@  Polymorphism

@  eCTD submissions

 

Course duration: 6 months,Sunday batches

 

Certification: Will be issued after successful completion of the course

 

Who can apply? Industry professionals & fresh B.Pharm/Graduates from suitable stream

 

For admissions, please contact: 

 Inline image 29619301401/ 9320049805/0251-2860207

Inline image 3 infopharmainstitute@gmail.com, Log on to www.ipmindia.net 

 

Best regards,
Ms.Sheetal Mohidekar,
Project Manager 
Institute of Pharmaceutical Management.
www.ipmindia.net
O: 0251-2860207
M: 9320049805
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Sudhakar Vaddi  |  24-Oct-2016 16:30:18 IST
I have total 5 years of experience in Quality Assurance department. I want to do Diploma course which is beneficial to my professional career and growth opportunities. Provide the guidance and course details and relevant information.
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