A WHO SHOULD
The Professional Expert Course Records and Regulatory Affairs is aimed at graduates and university graduates in the area of Health Sciences and Allied Workers (Pharmacy, Chemistry, Biology, etc.) or students coming to their qualifications, as well as professionals recently joined the pharmaceutical industry interested in acquiring a specialization that allows them to implement their professional activity in that sector.
The objective of Professional Expert Course Records and Regulatory Affairs It is to provide students with a comprehensive, deep and practical insight into all aspects of the rules governing the registration of medicines, both nationally and internationally as well as all the necessary technical requirements for the marketing authorization of the products with all health and in the shortest time possible.
750 hours. 45 virtual classrooms, virtual tutorials 5 hours, 450 hours of personal work and 250 hours for the manufacture of the final project.
For the duration of the course, each student will have access through the Virtual Campus, to all relevant documentation to the areas scheduled. It all contents of study and supporting materials necessary for the proper development of the course is included.
Each student will carry out various practical work related to the main areas of the course to be subsequently evaluated by the Program Manager.
PROGRAM OF CONTENTS
The Program Professional Expert Course Records and Regulatory Affairs It is structured in five main areas in order to cover all necessary aspects for complete formation of the student.
INTRODUCTION TO REGISTER
The contents of this first block forms the basis of the course program, it is a key to understanding the rest of the block element.
This first block structure as follows:
- Drug Registration applies to legislation.
- Functions Registration Department.
- Structure and Organization of the Health Authorities:
Spanish Agency for Medicines and Health Products (AEMPS), European Medicines Agency (EMA) Food and Drug Administration (FDA).
- Types of drugs and dispensing conditions.
- Phases of Drug Registration.
With this module, the student will have knowledge in:
- pharmaceutical legislation applied to Records / Regulatory Affairs both nationally and internationally.
- the role of the department of records within a pharmaceutical company.
- all health authorities involved in the evaluation and authorization of medicinal products.
- all steps to obtain authorization for a medicine.
- at the regulatory level differences between generic medicines, innovative, traditional herbal medicine, etc. Medicinal products subject to medical prescription. Medicinal products not subject to medical prescription. drugs excluded from financing (EXO). full, bibliographic, well established use dossier, etc ...
In this second block is one of the densest as it goes into detail on such important aspects as the preparation of all necessary to obtain the authorization of medicines, preparation of technical specifications, brochures and labeling tools employed with the Health Authorities Documentation for presentation and dispatch of documentation and publicity.
This second block is structured as follows:
- Preparation of Electronic Application Form (e-AF).
- Preparation of Electronic Records: eCTD (Electronic Common Technical Document) and / or NeeS (Non-eCTD Electronic Submissions).
- tools applied in drug registration: RAEFAR II, CESP, CIMA, Labofar, PMRD, etc ...
- Extended Medicinal Product Dictionary (XEVMPD): Eudravigilance.
- Drug Master File (DMF) / CEP: Open Party and Charter Access closed.
- Drug labeling and telematics management techniques and prospects tab.
- Advertising Drug / Health / Supplements and Cosmetics Alimentios.
With this module, the student will have knowledge in:
- Development of drug registration dossier. eCTD (Electronic Common Technical Document) and / or NeeS (Non-eCTD Electronic Submissions).
- Preparation of Electronic Application Form (e-AF): Administrative data.
- Technical Documentation of active ingredients. Drug Master File:
open and closed part. Letter of access.
- Management of databases / tools necessary for filing and sending documents to the Health Authorities.
Introduction of drug information and its corresponding update in the Dictionary of Medicines of the European Medicines Agency (EMA).
- Development of technical specifications, package insert and labeling of medications.
telematic management techniques and prospects chips during the authorization process of a new drug and variation of the marketing authorization that involves a modification of the texts.
- Drug advertising requirements and other legal grounds:
administrative procedures with the regions.
TYPES OF REGISTRATION PROCEDURES
The third section goes into detail about the types of existing procedures for the authorization of medicinal products. This third block is divided into:
- National procedure.
- Decentralized Procedure / MRA.
- Centralized Procedure.
With this module, you will learn to:
- Getting the marketing authorization of medicines by national procedure.
- Getting the marketing authorization of medicines by European procedure: mutual, decentralized and centralized recognition.
OTHER ACTIVITIES REGULATORY
The fourth block is to learn all the regulatory activities performed in the Records Department / Regulatory Affairs for the maintenance and updating of authorizations for medicinal products authorized.
This block is divided into:
- Registration variations.
- Five-year renewal. Cancellation of a marketing authorization.
Temporary suspension. Free Samples request. Notifications on the marketing of medicines for human use. Certificate application pharmaceutical.
- Export and import of medicines.
- Opening authorization of pharmaceutical laboratories and their modifications.
- Prices and Financing of Medicinal Products.
With this module the student will learn:
- Updating authorizations for medicines. Registration variations.
- Other important regulatory efforts to maintain authorizations.
- As authorization for the opening of a laboratory owner, manufacturer or imported and their dealings with the health authorities is requested.
- Procedures for import and export procedures and obtaining certificates of drugs.
- Handling procedures financing and pricing of medicines by the National Health System. telematic application of the Ministry of Health: GESFARMA. Reference prices. Homogeneous groups.
In this last block, other legal bases that are managed in the departments of laboratory records applied to medical devices, food supplements, cosmetics and personal care products are addressed.
The block is divided into:
- Medical devices.
- Food Complements.
- Cosmetics and Personal Care Products.
With this fifth block, students will learn:
- in medical devices: Product record. Distribution and manufacture of medical devices. Obtaining the CE marking. Market surveillance. Labeling of medical devices.
- in food supplements: Notification of placing on the market. Sanitary registration. Authorization of facilities. Labeling of Dietary Supplements.
- In cosmetics and personal care products: Notification of placing on the cosmetics market in the CPNP. Labeling of cosmetics. Application National Code. Application for Certificate of Free Sale (CLV).
PROFESSIONAL CAREER ASSISTANCE
Within the educational philosophy of CESIF and as a training supplement, CESIF ON LINE offers its students after satisfactory completion of their training period, the possibility of having the services of a Professional Career Assistance (specialized in Online Job Search Consultant) which periodically send each student those job offers that fit your profile and are considered attractive for the development of his career.
Course of Professional Expert in Drug Registration and Regulatory Affairs is designed to fully develop the professional skills of students in all areas of specialization theoretical and related departments Records / Regulatory Affairs of pharmaceutical companies worldwide practices.
Among the sectors include:
- pharmaceutical laboratories.
- Health sector consulting.
- Medical device companies.
Within the functional areas of development are:
- Validations / Revalidations.
- Regulatory Affairs.