# Pharma Regulatory Institute > in Noida ## Posts - [A career in drug regulatory affairs can be rewarding and fulfilling, with many benefits & advantages including:](https://pharmaregulatoryinstitute.com/2023/09/29/roles-responsibilities-of-drug-safety-associate-or-pharmacovigilance-associate-3/): Making a differenceDrug regulatory affairs professionals ensure that patients have access to safe and effectivedrugs.  Job security and growthThe pharmaceutical industry is growing rapidly, and there is a high demand for regulatoryaffairs specialists.  Competitive salaryRegulatory affairs professionals are in high demand and receive competitive salaries.  FlexibilityOnline courses allow you to study at your own pace from anywhere in the world.  Interdisciplinary collaborationYou can work with experts from various disciplines and gain insights from differentperspectives.  Intellectual stimulationThe work is constantly evolving, keeping it engaging and challenging.  Sense of purposeKnowing that your work directly impacts public safety can be highly rewarding.  In-depth… - [Roles & Responsibilities Of Drug Safety Associate Or Pharmacovigilance Associate](https://pharmaregulatoryinstitute.com/2023/09/29/roles-responsibilities-of-drug-safety-associate-or-pharmacovigilance-associate-2/): A Drug Safety Associate is a professional who works in the field of pharmacovigilance…. - [Roles & Responsibilities Of Drug Safety Associate Or Pharmacovigilance Associate](https://pharmaregulatoryinstitute.com/2023/09/29/roles-responsibilities-of-drug-safety-associate-or-pharmacovigilance-associate/): A Drug Safety Associate is a professional who works in the field of pharmacovigilance…. ## Pages - [Registration-payment-links](https://pharmaregulatoryinstitute.com/registration-payment-links/): Attach the payment receipt and upload the scanned copy while filling out the form below. Enter Your Detail - [Registration-payment-link](https://pharmaregulatoryinstitute.com/registration-payment-link/): Attach the payment receipt and upload the scanned copy while filling out the form below. Enter Your Detail - [Free Registration](https://pharmaregulatoryinstitute.com/free-registration/): FREE REGISTRATION - [Free Brochure Download](https://pharmaregulatoryinstitute.com/free-brochure-download/): Free Brochure Download Home Please Fill The Form To Download Free Brochure - [Register](https://pharmaregulatoryinstitute.com/register/): Register Home Please register for a free demo class on Drug Regulatory Affairs (DRA) and Pharmacovigilance (PV) every Friday @11.00am - [Corporate Solutions](https://pharmaregulatoryinstitute.com/corporate-solutions/): Corporate Solutions Home Corporate Solutions Established in 2007, ACPL offers wide range of training solutions and CMEs for the pharmaceutical companies, CROs, consulting firms, hospitals and NGOs. ACPL has experience of providing training and corporate solutions/services in the following areas. Executive hands-on training (DRA/PV) : Corporate executive training program in Regulatory Affairs & Pharmacovigilance Drug Regulatory GCP, GMP & GLP, CMC, CTD, eCTD, Submission Package, Manufacturing & Loan Licences, Medical Device Registration Services Food, Cosmetic licences Pollution/Fire NOCs Insecticides and Pesticides Certification, Custom Clearance Pharmacovigilance Case Processing [ICSRs], Med Info Contact Centre Oracle based software – ARGUS, ARIS g, Clinevo,… - [Gallery & Images](https://pharmaregulatoryinstitute.com/gallery-images/): Gallery & Images Home - [Contact Us](https://pharmaregulatoryinstitute.com/contact-us/): Contact Us Home Head Office B-3, B Block, Sector 6, Noida, Uttar Pradesh 201301 Phone +91-9266665201 +91-9266665230 Email info@pharmaregulatoryinstitute.com info@acplgroupindia.co.in Send a message - [Courses](https://pharmaregulatoryinstitute.com/courses/): Courses Home Drug Regulatory Affairs (DRA) DRA professionals are the connecting link between the concerned regulatory bodies and the pharmaceutical industries. PRI molds the students towards professional areas which directly belong to competitive markets in the field of drug regulatory at the global level to fit automatically into the required position easily. Read More Pharmacovigilance (PV) Pharmacovigilance Training Program: Good Health is the most expensive and precious aspect of life and therefore is the first priority of the human being. Experts from the pharmacovigilance team keep watch on the use and the adverse effects shown by the drugs present in… - [Certification](https://pharmaregulatoryinstitute.com/certification/): Certification Home - [Accreditation](https://pharmaregulatoryinstitute.com/accreditation/): Accreditation Home - [Experienced Faculty](https://pharmaregulatoryinstitute.com/experienced-faculty/): Experienced Faculty Home Mrs. Sharda Parashar Sr. Faculty-Regulatory affairs Experience: 10+yrs. Mrs. Rubi Kumari Sr. Faculty-Regulatory Affairs Experience- 10+yrs. Ms. Simran Rao Faculty-Regulatory Affairs Dr. Mantasha Manjer Sr. Faculty-Pharmacovigilance Experience- 7+yrs. Mrs. Arzoo Pannu Sr. Faculty-Pharmacovigilance Experience: 8+yrs. Mrs.Neha Gupta Advisor-Regulatory Affairs Experience- 9+yrs. - [Advisory Board](https://pharmaregulatoryinstitute.com/advisory-board/): Advisory Board Home Under the guidance of Mr. Prasad Bhat Chairman-ACPL Group of Companies Mr. Bhrigu Kaul Associate Vice President Experience- 25+yrs. Mr. Deepak Sharma Advisor-Pharmacovigilance Experience- 11+yrs. Mr. K. M. Dineshan Sr. Consultant Experience 30+years - [Certification Program in Pharmacovigilance](https://pharmaregulatoryinstitute.com/certification-program-in-pharmacovigilance/): Certification Program in Pharmacovigilance Home Pharmacovigilance (PV) Pharmacovigilance Training Program: Good Health is the most expensive and precious aspect of life and therefore is the first priority of the human being. Experts from the pharmacovigilance team keep watch on the use and the adverse effects shown by the drugs present in the market. This way the pharmacovigilance team monitors and guides about the rational use of the drugs. Topic covered in Pharmacovigilance (PV) Introduction to Pharmacovigilance Adverse drug reactions and safety reports Pharmacovigilance regulatory requirements Methodologies in Pharmacovigilance Pharmacovigilance process flow Aggregate reporting Signal management Pharmacovigilance of:- Medical Devices –… - [Certification program in Drug Regulatory Affairs](https://pharmaregulatoryinstitute.com/certification-program-in-drug-regulatory-affairs/): Certification program in Drug Regulatory Affairs Home Drug Regulatory Affairs (DRA) DRA professionals are the connecting link between the concerned regulatory bodies and the pharmaceutical industries. PRI molds the students towards professional areas which directly belong to competitive markets in the field of drug regulatory at the global level to fit automatically into the required position easily. Topic covered in Drug Regulatory Affairs (DRA) • Introduction to DRA • Introduction to DRA documentation• Governing regulatory authorities across the globe• The WHO-ICH guidelines• Detailed Study of Drug & Cosmetic Act & Rule, 1940, India. Rules in USA & EU• Detailed Study… - [Placements](https://pharmaregulatoryinstitute.com/placements/): Placements Home Placements & Testimonials We provides 100% placement assistance as a value added complimentary service to all students who has done courses in PRI. It is a right time to take a positive and smart decision by you to make a career in the highly technical & paying field of DRA & PV. After doing hands-on training from PRI you will be open to multiple Job opportunities for you. Our Clients Our Students Testimonial Vikram Singh Anata Medicare Limited Kunal Kumar Professional Utility Chetan Raj ELT Pvt. Ltd. Devansh Kulshreshtha Sofu Dental India Pvt. Ltd. Sandhya Kumari Sofu Dental… - [Student Information Center](https://pharmaregulatoryinstitute.com/student-information-center/): Student Information Center Home Orientation Program In Drug Regulatory Affairs & Pharmacovigilance DURATION Day 1 : 1.5 hours per lecture. Total of lectures spread over morning and afternoon sessions. Day 2 : 1.5 hours per lecture. Total of 2 lectures in the morning session.3 hours of interactive counselling and placement talk. TRAINERS Professional trainers from Industry Subject Matter expert in Drug Regulatory Affairs (DRA) and pharmacovigilance (PV) ELIGIBILITY B.Pharma 3rd & Final year students M.Pharma Students Bsc/Msc Microbiology, Biochemistry BDS & BAMS REGISTRATION FEES Registration Fees : Rs. 2000/- Two days program. A booklet covering important points of DRA &… - [About Us](https://pharmaregulatoryinstitute.com/about-us/): About Us Home About Us ACPL Group Of Company Accredited Consultants provide exceptional value to the clients by rendering top-quality; cost–effective, customized, innovative and timely completion of work in drug regulatory services. We take responsibility and accountability for project performance and strive to create a solution-based relationship. We are identified as one of the most reliable service providers in Drug Regulatory Consultancy services, Regulatory Training, jobs for the deserving candidates, Custom duty & Freight forwarding services are appreciated by our domestic as well as International clients. ACPL currently has clients in the USA, UK, China, Germany, Japan, Israel, Italy, Australia… - [Test](https://pharmaregulatoryinstitute.com/test/): # Car Repair High quality repair & maintenance It is beautifully designed in a very smart way to bring the best user experience that you will love. Get Appointment Watch Video Vehicle Inspection A small river named Duden flows by their place and supplies it with the necessary Expert Mechanics A small river named Duden flows by their place and supplies it with the necessary Quality Services A small river named Duden flows by their place and supplies it with the necessary Committed! Always deliver more than expected. Behind the word mountains, far from the countries Vokalia and groves Consonantia,… - [Home](https://pharmaregulatoryinstitute.com/): Pharma Regulatory Institute [PRI] About Our Institute PRI-Pharma Regulatory Institute is a division of Accredited-Consultants Pvt. Ltd. which was specifically established for imparting Academic and Professional Training focused on Drug Regulatory, Pharmacovigilance, Clinical Research, Medical Coding, Licensing, Custom Clearance, HR, Legal Documentation, Good Distribution Practices, Logistics, Food & Safety Regulations, Agriculture & Animal Husbandry and others, such as Office Administration & Management, Personality Development, Interview Training etc. PRI is also working as a consultant to the student to obtain admission in the Field of Pharmacy, Pharma-Management, Medical, Para-Medical, Engineering, BBA, MBA, BCA, MCA, Polytechnic, Ph. D, Biotechnology, Bioinformatics, LLB, Architecture,… - [Sample Page](https://pharmaregulatoryinstitute.com/sample-page/): This is an example page. It’s different from a blog post because it will stay in one place and will show up in your site navigation (in most themes). Most people start with an About page that introduces them to potential site visitors. 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