Nashik

Admission open in MBA Pharmaceutical Management at IIHMR University - Scholarships available

PROGRAM OVERVIEW
The University offers MBA Pharmaceutical Management. This educational program aims at developing trained professionals with requisite skills in planning and operating management techniques; diagnosing and solving management problems; and acquiring consultancy skills, with a view to preparing them to manage pharmaceutical industrial units. The in-take capacity of the program is 60.


Clinical Research & Pharmacovigilance: Make your career with an IGMPI's accredited PG Diploma

INSTITUTE OF GOOD MANUFACTURING PRACTICES INDIA
Global accredited training & certification provider
Conferred with QUALITY COUNCIL OF INDIA (QCI) – D.L. SHAH NATIONAL QUALITY AWARD & ASSOCHAM Services Excellence Award 2017

New Delhi | Noida | Vadodara | Distance cum e-Leaning

Trusted by organizations & training participants in over 30 countries
Training | Certification | Education | Research

www.igmpiindia.org

 www.ffsqindia.org  |  www.fcrindia.org | www.fhaindia.org | www.amciindia.org


Glimpse of Programmes:

Post Graduate, Executive Diploma and Industry Certificate Programmes in Pharma/Food:

(Duration: 3-12 months)

Faculty of Clinical Research

  • Clinical Research
  • Pharmacovigilance 
  • Medical Writing
  • Clinical Data Management

Faculty of Good Manufacturing Practice    

  • Good Manufacturing Practices
  • Quality Assurance and Quality Control (Drug as major)
  • Regulatory Affairs (Drug as major)
  • Quality Assurance and Quality Control (Medical Device as major)
  • Regulatory Affairs (Medical Device as major)
  • Computer System Validation
  • Good Laboratory Practices

Faculty of Drug Discovery and Development

  • Pharmaceutical Chemistry
  • Drug Discovery and Development
  • Bioinformatics
  • Pharmaceutical Formulation and Entrepreneurship

Faculty of Product Management

  • Pharma Product Management
  • Pharmaceutical Sales and Marketing Management
  • Pharmaceutical Technology Transfer
  • Food Product Management
  • Food Supply Chain Management
  • Pharmaceutical Packaging
  • Pharmaceutical Process Engineering
  • Biopharmaceutical Technology
  • Big Data Analytics

Faculty of Healthcare Administration

  • Public Health and Hospital Management
  • Healthcare Informatics
  • Medical Device Management
  • Medical Records Technology

Faculty of Intellectual Property Rights

  • Intellectual Property Rights

Academy of Medical Coders India

  • Medical Coding
  • International Classification of Diseases (ICD-10-CM)
  • Clinical Documentation Improvement (CDI)
  • CPC Examination Training
  • Medical Record Technology

Faculty of Nanotechnology

  • Pharmaceutical Nanotechnology

Faculty of Health Safety and Environment

  • Health Safety and Environment

Faculty of Food Safety and Quality 

  • 2 Years M.Sc. (Food & Nutrition) / (Dietetics & Applied Nutrition) + PGD in Nutrition & Dietetics
  • Food Analysis and Quality Assurance
  • FSSAI Food Safety Supervisor
  • Food and Agribusiness Management
  • Food Quality Assurance and Quality Control
  • Food Processing and Preservation
  • Food Good Laboratory Practices
  • Food Good Manufacturing Practices
  • Food Regulatory Affairs
  • Food Safety
  • Food Product Management
  • Food Sales and Marketing Management
  • HACCP Certification
  • Clinical Nutrition (Industry Certification)
  • Food Safety Management Systems (Industry Certification)
  • Nutrition and Dietetics
  • Nutraceuticals
  • Probiotics in Food
  • Organic Farming and Food Production systems
  • GAP Certification
  • Food Safety in Hospitality Industries
  • Food Supply Chain Management
  • Food Packaging
  • Bakery and Confectionery
  • Bakery Science and Technology
  • Dairy Science and Technology
  • Certified FSMS Lead Auditor
  • Diploma in Food Processing
  • Hospitality and Hotel Management
  • Food Science and Technology

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Professional Certification in (Pharma): Certified Pharmaceutical GMP Professional, Certified Pharmaceutical Quality Manager, Certified Pharmaceutical Quality Auditor, Certified Pharmaceutical Quality Technician, Certified Drug Regulatory Affairs Professional, Certified Medical Device Professional, Certified GMP for Medical Devices Professional, Certified GMP for Combination Products Professional, Certified GMP for Blood and Blood Components Professional, Certified GMP for Biological Products Professional, Certified GMP for Cosmetics Professional, Certified GMP for Herbal Medicines Professional, Certified GMP for Herbal Medicines Professional, Certified WHO - GMP Professiona, Certified Data Integrity Professional, Certified Quality by Design (QbD) Professional, Certified Quality Risk Management Professional, Certified Medical Device Professional (CMDP), Certified Good Clinical Practices (GCP), Certified Good Laboratory practice professional(CGLPP)

Professional Certification in (Food): FSSAI Food Safety Supervisor, Certified Food GMP Professional, Certified Food Quality Manager, Certified Food Quality Auditor, Certified HACCP Auditor, Certified Regulatory Affairs Professional, Certified Food Quality Technician, Certified Validation Professional, Certified Quality Risk Management Professional, Certified FSMS Internal Auditor and Certified FSMS Lead Auditor.

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Certificate Programmes (1-3 Months duration): GMP for Finished Pharmaceuticals & Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs, GMP In Manufacturing, Packing, or Holding Human Food, Food and Drug Regulatory Agencies, Process Analytical Technology , Documentation in QA & QC Department, Registration of Drug and Dossier Preparation (CTD and eCTD submissions), Drug Registration (European market), Drug Registration (GCC countries), Drug Registration (African countries), Drug Registration (India), Drug Registration (US Market-ANDA, NDA etc), Preparation and Submission of Drug Master File (DMF) and Prescription to OTC Switch, Medical Sales Representative, Computer System Validation, Computer Aided Drug Design (CADD), Pharmaceutical Validation

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Modes available:
Full Time Class Room Programmes
Part Time Class Room programmes (Weekend classes)
Distance cum e-learning mode (Comprehensive study material along with lectures on LMS)

For PDF copy of the Prospectus & Application form, write to info@igmpiindia.org mentioning the name of the course and your phone number.

 

Program Highlights:

  • Approved by Quality Council Of India
  • Accredited Vocational Institution of Ministry of HRD, Government of India
  • Affiliated with Life Sciences Sector Skills Council (SSC) and Food Industry Sector Skills Council set up by National Skill Development Corporation (NSDC).
  • IGMPI Certifications demonstrate your professional accomplishment and proficiency leading towards professional credentialing
  • Selection will be based on the student's/participant’s profile.
  • Placement assistance by a robust placement cell to carve out a niche career path for the students.
  • Post Graduate Diploma is 6-12 months 'duration programme while Executive Diploma and Industry Certificate programmes are advanced and fast-track programme of 3 to 6 months' duration. Certificate programme is advanced programme of 1 month duration.
  • Practical experience provided along with theoretical knowledge to give complete understanding of subjects.
  • Government of India Approved & ISO 9001:2008 certified laboratory facility.
  • A team of experts with an industrial experience of 35-40 years and a competent work profile have been engaged as faculty members.
  • E-lectures through Learning Management System (LMS) help the students in their learning process.
  • Comprehensive, dynamic and advanced study material with an international perspective and case study based approach.
  • A fee concession of 10% is applicable to candidates belonging to SC/ST/Physically handicapped /weaker section/Ex-Serviceman/Defense Personnel (or their progeny)

 

Eligibility:
Life Science graduate / B.Pharm / M.Pharm / M.Sc / Ph.d in science disciplines/ any diploma holder or passed outs of Clinical Research degree or diploma courses ,Food science, Food Technology, Food Manufacturing, Food Quality Assurance, Home Science, Agriculture, Management Professionals, Testing, Audit Microbiology professionals, are eligible for these course. Working professionals of any of the following industry types Drugs manufacturing, Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic, Food, Manufacturing, Biotechnology or any related industry are highly encouraged to apply for the programme.

 

Placement details and Participation from Pharma, Food & healthcare giants around the globe:
In the last batch, the Institute has witnessed participation of more than 1500 students and professionals now working with Fortune 500 and global healthcare & Pharmaceutical giants like Dr. Reddy’s Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Dabur, DS Group, Fortune, Mother Dairy, Reliance Fresh, SGS,Marico, Pepsi, Elite,Parle, Nestle, Capricorn, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Biocon etc.

 

IGMPI Accreditation:

  • Approved by Quality Council of India (QCI), Government of India
  • Accredited Vocational Institution of Ministry of HRD, Government of India
  • Approved Training Institute of Food Safety and Standards Authority of India (FSSAI)
  • Recognized by Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India
  • Affiliated with Life Sciences Sector Skills Council (SSC) and Food Industry Sector Skills Council set up by National Skill Development Corporation (NSDC)
  • Registered under the Societies Registration Act, 1860, Government of India
  • A PMKVY (Pradhan Mantri Kaushal Vikas Yojana) affiliated training partner.
  • Empanelled under ministry of Horticulture and Food Processing, Government of Uttar Pradesh
  • An ISO 9001: 2015 Certified Institute accredited under Dubai Accreditation Center (DAC), UAE
  • International Register of Certificated Auditors (IRCA) accredited Lead Auditor (FSMS) course
  • Conferred with QUALITY COUNCIL OF INDIA (QCI) – D.L. SHAH NATIONAL QUALITY AWARD & ASSOCHAM Services Excellence Award 2017

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Contact us:
Get in touch with our experts for technical counselling or for prospectus on +91 8130924488, 8587838177, +9120 2427175, 4375280 / info@igmpiindia.org mentioning the name of the Course and your phone number

New Delhi | Noida | Vadodara

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Become a certified clinical research and PVG professional

Catalyst Clinical Research Services
Leading Clinical Research and Pharmacovigilance Training Providers

www.catalystclinicalservices.com

info@catalystclinicalservices.com

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Now, you can boost your career growth by becoming a certified clinical research and pharmacovigilance professional. You can learn effective good clinical practices, clinical trials and pharmacovigilance skills by participating in one or more of the courses listed below:

  1. Professional Diploma in Clinical Research (PDCR)
  2. Professional Certificate in Pharmacovigilance (PCPV)
  3. Certificate Program in Scientific Writing (SW)
  4. Certificate Program in Project Management (PM)
  5. Certificate Program in Clinical Trial Management (CTM)
  6. Oncology Clinical Trials Training (OCTT)

With a participation of more than 9000 candidates across 27 countries over the last 14 years, these courses have received wide acclamation from the key stakeholders. Majority of the successful participants are employed across 300+ organizations.

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Professional Diploma in Clinical Research (PDCR)
Duration:
6 months; Eligibility: B.Pharm 3rd year onwards; Fee: Rs. 9600
Module-1: Introduction to Pharmaceutical Medicine

  • The Drug Development Process
  • New Drug Discovery
  • Clinical Development of Drug
  • Essential Clinical Trial Documents
  • Clinical Trials Terminology

Module-2: Good Clinical Practice (GCP) Foundations

  • History of GCP - milestones in the evolution of GCP
  • Principles of GCP and applicable GCP Guidelines
  • Declaration of Helsinki
  • Clinical Study Process
  • The Management of Clinical Studies (Sponsor)
  • Ethics in Clinical Research
  • Informed Consent
  • Serious Adverse Event (SAE)
  • Challenges in the Implementation of GCP Guidelines
  • Biostatistics

Module-3: Drug Regulatory Affairs (Clinical Trials)

  • Overview of Regulatory Environment in USA, Australia, Europe and India
  • Clinical Trial Application Requirements in India
  • Import-Export of Clinical Trial Drugs in India
  • Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule.
  • IND/ANDA/New Drug Application

Module-4: Roles and Responsibilities of Clinical Trial Personnel

  • Roles and Responsibilities of Sponsor
  • Roles and Responsibilities of Investigator
  • Roles and Responsibilities of ERB/IRB/IEC
  • Roles and Responsibilities of CRA /Monitor/Auditor/ Clinical Research Coordinator
  • Roles and Responsibilities of CRO
  • Roles and Responsibilities of Regulatory Authorities
  • Roles and Responsibilities of Clinical Data Manager (CDM )
  • Roles and Responsibilities of Clinical Biostatistician

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Professional Certificate in Pharmacovigilance (PCPV)
Duration:
6 months; Eligibility: B.Pharm 3rd year onwards; Fee: Rs. 9600

Training Topics:

  • Introduction to Pharmacovigilance (PV) and Risk Management
  • Standard Terms and Definitions
  • Global Perspective of PV and ADR Reporting

- Basic Steps in Setting-up PV Centre
- How to Join WHO NPP
- Practical Procedure for Joining WHO Drug Monitoring Program (ASCoMP)
- Pharmacovigilance Methods

  • Guidelines and Standard Governing PV-ICH Guidelines, US FDA Guidelines, CFR, EU Guidelines, CIOMS Guidelines
  • Global AE reporting System and Reporting Forms

- Introduction and Definition of AE
- Introduction and Aspects Related to AE Reporting
- Pre and Post Marketing Approval of a Drug
- AE Reporting Procedure
- AE Reporting Form

* US FDA Form 3500 and 3500A
* Vaccine Adverse Event Reporting System (VAERS)
* Medicines and Healthcare Products Regulatory Agency’s Vigilance Reporting Form
* Medeffect Canada and Canada Vigilance Program
* Suspected Adverse Drug Reaction Reporting (SADRR) Form
* Universally Accepted ADR Reporting Form CIOMS I Form
* Therapeutic Good Administration Australian Vigilance System –Blue Card

  • Individual Case Safety Reports (ICSRs)
  • Medical Directory for a Drug Regulatory Activities (MedDRA)
  • Periodic Safety Update Reports (PSURs)
  • Expedited Reporting and Requirements
  • PV Inspection and Compliance Monitoring

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Highlights of Training Courses:
* Ease of training (distance learning)
* Assignment based evaluation
* Optimal course fee
* Hand-on practical training component
* Industry-wide recognition
* Placement assistance via job openings on WhatsApp almost on daily basis
* Successful participants employed across 300+ organizations

Kindly get in touch at +91 9818356273 or mail at info@catalystclinicalservices.com to get further details of the courses.

Catalyst Clinical Services Pvt. Ltd.
Unit No. 11, CSC-12, Block-D1, Sector-16, Rohini, Delhi - 110089
M: 9818356273, 8826806862 (voice call and WhatsApp)
Email: info@catalystclinicalservices.com
Leading Clinical Research and Pharmacovigilance Training Providers

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Start your career in Clinical Research. Join India's leading Clinical Research Institute. Admissions Open for 20th FEB & 20th MARCH 2018 batch

Clinical Research, Clinical Data Management and Pharmacovigilance training Institute
Hyderabad | Bangalore | Pune | Nagpur | Mumbai
www.cliniindia.com


Are you ready to step into Clinical Research Industry? Do you want to do a full-fledged Advanced Program from Clini-India !

WE ARE DEDICATED FOR YOUR TRAINING AND CAREER DEVELOPMENT

 

Clinical Research Industry is all set to become the next big demanding career in India. A large population with a substantial workforce and cost benefits influence multinationals to set up research facilities here. Besides due to the prevalence of a large variety of diseases, including widespread cases of cancer and diabetes India.

 

<<<CLICK HERE TO KNOW MORE>>>

 

Who we are?
CLINI INDIA – India’s First Award winning Clinical Research Institute for Best Placements in Clinical Research Industry. We are offering advanced training in following sector.

VISIT OUR WEBSITE - www.cliniindia.com

Program: Join Advanced Program in Clinical Research and Management

Modules:

  • Clinical Research
  • Clinical Data Management
  • Pharmacovigilance
  • Medical Writing

Duration: 4 Months

Program Mode: Full time / Weekend / Online classes

 

UPCOMING BATCHES

Book your seat today !

CAMPUS JAN FEB MAR
Bangalore 20th Feb 20th Mar 17th Apr
Hyderabad 20th Feb 20th Mar 17th Apr
Pune 20th Feb 20th Mar 17th Apr
Mumbai 25th Feb 25th Mar 29th Apr

CLICK HERE TO FILL FORM TO GET A CALL FROM OUR EXPERTS

 

Inclusions:

  • Training Session by Certified Industry Subject Matter Experts.
  • Globally recognized Program Content and Course Materials.
  • Case Studies.
  • No Examination processing charges.
  • Practical exposure on CDM and Pharmacovigilance tools.
  • Program Certification.
  • Placement Assistance.
  • Resume Development.
  • Soft Skills / Communication Training.
  • Interview Preparation / Pre-recruitment training.
  • All Necessary Stationary.
  • Exclusive Discount Vouchers for future Learning.
  • Referral support for quick placements.
  • Clini India Goodies and more

 

Placement details: (Click here to know our placements records)

In the last batch, the Institute has witnessed participation of many Life Science students and professionals now working with Fortune 500 and global CRO, Pharma and IT Companies  more details - Click here

 

Bangalore Hyderabad Pune Mumbai
No.104 EPIP Zone, Whitefield,
2nd Floor, Prestige Omega,
Bangalore, KA 560066
Swathi Plaza, Behind Honda Showroom,
Near Yashoda Hospital,Somajiguda ,
Hyderabad  500082
6th Floor, Pentagon 2,
Magarpatta City,
Hadapsar,
Pune, Maharashtra 411013
1st Floor, HDIL Kaledonia,
Sahar Road, Andheri East
Mumbai 400069
Phone - 8050040004 Phone - 8886904030 Phone - 7066457703 Phone - 9758644222

 

<< CLICK HERE, IF YOU WISH TO GET PROGRAM DETAILS >>

<<CLICK HERE TO VISIT WEBSITE>>

[OUR PLACEMENTS]

[STUDENTS TESTIMONIALS]

 


Walk in interview in Quality Control, Quality Assurance, Production, Microbiology at Glenmark

Glenmark is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity) with eight molecules in various stages of clinical development. The company has a significant presence in branded generics markets across emerging economies including India. Its subsidiary, Glenmark Generics Limited has a fast growing and robust US generics business. The subsidiary also markets APIs to regulated and semi-regulated countries. Glenmark employs nearly 6000 people in over 80 countries. It has twelve manufacturing facilities in four countries and has five R&D centres.


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