Surat

Wanted Stores Incharge / Assistant at SDPC

Shree Dhanvantary Pharmacy College (SDPC), established in 2005 by Shree Sahkar Education Trust, Surat.  During this brief tenure of eleven years, it has made rapid strides of progress to become one of the premier institutes of Pharmacy in Gujarat. This institute is approved by AICTE, PCI & affiliated to GTU and currently offering B.Pharm, M.Pharm (Pharmaceutical Chemistry, Pharmaceutics, Pharmacology & Quality Assurance), Pharm.D. & Ph. D. courses.

Post : Stores Incharge / Assistant


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.


Recruitment for Professor at Shree Dhanvantary Pharmacy College | 07 posts

Shree Dhanvantary Pharmacy College (SDPC), established in 2005 by Shree Sahkar Education Trust, Surat.  During this brief tenure of eleven years, it has made rapid strides of progress to become one of the premier institutes of Pharmacy in Gujarat. This institute is approved by AICTE, PCI & affiliated to GTU and currently offering B.Pharm, M.Pharm (Pharmaceutical Chemistry, Pharmaceutics, Pharmacology & Quality Assurance), Pharm.D. & Ph. D. courses.

Post : Professor


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.

ENQUIRE for Professional certification >>

 

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

ENQUIRE for Certificate programs  >>

 

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

ENQUIRE NOW

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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Job for M.Pharm, M.Sc, B.Pharm in Quality Assurance at Ribosome Research Center

Shree Dhanvantary Pharmaceutical Analysis and Research Centre (SDPARC) is a contract research organization established in 2006 and is managed by RIBOSOME PHARMA PVT. LTD., Surat. SDPARC offers a wide range of analytical & research services for small, medium and large scale pharmaceutical, ayurvedic, bulk drug, chemical, food and cosmetic industries. The centre is approved by the Food and Drug Control Administration (FDCA), Gujarat state as a public testing laboratory and is spread over 8,000 sq. ft. area. The centre is equipped with state of the art analytical facilities to cater to the needs of our clients and provides accurate, prompt and cost-effective analytical services in compliance with cGMP, GMP and various pharmacopeia guidelines.

Post : QA


BANKRUPTCY IN PHARMACEUTICALS

ABOUT AUHTORS
Rajesh Vagh
PharmaTutor Edu Labs
Surat, Gujarat
rajesh@pharmatutor.org

Bankruptcy may be a new term or less familiar with most of you but it is of higher importance. Bankruptcy is a legal status of a person or other entity that cannot repay debts to creditors. We may consider it as a white-collar fraud. First let me clear that bankrupt can be defined as different act in various jurisdiction but generally  bankruptcy statutes involve concealment of assets, concealment or destruction of documents, conflicts of interest, fraudulent claims, false statements or declarations, and fee fixing or redistribution arrangements etc.  Bankruptcy fraud is a federal crime in the USA and India.


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

ENQUIRE NOW>>


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.

ENQUIRE NOW>>

 

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

ENQUIRE NOW>>

 

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

ENQUIRE NOW>>


Job for M.Pharm, B.Pharm in Quality Assurance at Envision Scientific | Fresher apply

Envision Scientific Pvt. Ltd. is a leading provider of drug delivery technologies to the healthcare industry. Our developed technologies are designed to be utilized for various types of drug and different delivery systems. Its proprietary NANO ACTIVETM Technology is designed for drug delivery utilizing Nanotechnology from various types of devices and surfaces. We Vision ‘To have a Happy and Healthy World’.

Post : Quality Assurance


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