Pharmacology & Regulatory Affairs

Transcription

1 2 nd International Conference & Expo on Pharmacology & Regulatory Affairs August, 2018 Berlin, Germany Theme Cutting Edge Research Works in Pharmacy & Drug Development

2 About Conference: Cenetri Publishing Group reunite all the participants around the world to join the 2 nd International Conference and Expo on Pharmacology & Regulatory Affairs with the theme of Cutting Edge Research Works in Pharmacy & Drug Development scheduled at Berlin, Germany. It is a broad-based topic founded on two key tenets: To explore the most exciting researches with respect to the subjects on Pharmaceutical Regulatory Affairs: Secondly, to provide a rapid turn-around time possible to research, teaching and reference purposes. This conference will provide the finest platform where you can deliberate the prominence of pharmacology & regulatory affairs that covers research on the toxicological an pharmacological effects of environmental contaminants, pharmacologic concerns on both experimental and clinical levels, clinical toxicology, pharmacokinetics, pharmacodynamics, drug interactions, collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. Scope and Importance: Pharmacology is the branch of medicine concerned with the uses, effects and modes of action of drugs. It studies how different chemicals affect biological systems, and incorporates knowledge and skills from a number of basic science disciplines including physiology, biochemistry, and cellular and molecular biology. The Regulatory Affairs department is an important part of the organizational structure of pharmaceutical companies. Internally it liaises at the interphase of drug development, manufacturing, marketing and clinical research. Externally it is the key interface between the company and the regulatory authorities. It is actively involved in every stage of development of a new medicine and in the post-marketing activities with authorized medicinal products. The scope of pharmacology is rapidly expanding and provides the rational basis for the therapeutic use of the drug. The success of regulatory strategy is less dependent on the regulations than on how they are interpreted, applied, and communicated within companies and to outside constituents. Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing as the drug development process is a lengthy, complex and extremely costly albeit necessary process. Pharmacology has a wide scope, and derives from various other disciplines like physiology, microbiology, pathology, biochemistry and various clinical specialties. Prominent scientific sessions: Advances in Pharmacology Clinical Pharmacology Pharmacogenomics Pharmacokinetics Pharmacoepidemiology Pharmacotherapy and Posology Neuropharmacology Psychopharmacology Pediatrics Pharmacology Pharmacology & Toxicology Theoretical Pharmacology Behavioral Pharmacology Environmental Pharmacology Drug Design, Delivery and Formulation Bioequivalence and Bioavailability Adverse Drug Reaction and Treatment Clinical research and Drug Legislation Pharmacovigilance and Drug safety Pharmaceuticals and Personal Care Products

3 Target Audiences: Medical Doctors Physician Assistants Health Coaches Family Practice Doctors Licensed Herbalists Osteopathic Physicians Massage Therapists Dentists Naturopathic Physicians Chiropractic Physicians Who can attend? Academicians Researchers Healthcare Technology Providers Healthcare Professionals Pharma Industrialists Pharmacists Medical Directors Principal Investigators Acupuncturists Physical Therapists Homeopaths Hysician Assistants Advanced Practice Nurses Registered Nurses Physician Assistants Dietitians Nutritionists Midwives Pharmacists Methodologists and other Regulatory professionals along with Academicians Graduates and Post graduates in Industrial Pharmacy Medical Devices Manufacturing Companies, CRO Data Management Companies. Pharmaceutical legislators and regulators Toxicology Testing Companies & Organizations Why to Attend??? This conference provides the chance to Meet and network 100+ industry leaders and peers, with co-located events under Pharmacology and gain critical advises from industrial experts on the related regulation matters. To grasp and gain the quality information in terms of breadth and depth of key topics on production registration, submission, pharmacovigilance, clinical regulatory requirements and other topics with respect to the scientific sessions. To take the opportunity of exchanging, circulation and gaining the knowledge and ideas for the future prospects.

4 Registration Categories

5 About Berlin, Germany Berlin is the capital and the largest city of Germany as well as one of its 16 constituent states. With a steadily growing population of approximately 3.7 million. Berlin is the second most populous city proper in the European Union and the seventh most populous urban area in the European Union. Located in northeastern Germany on the banks of the rivers Spree and Havel, it is the centre of the Berlin-Brandenburg Metropolitan Region, which has roughly 6 million residents from more than 180 nations. Due to its location in the European Plain, Berlin is influenced by a temperate seasonal climate. Around one-third of the city s area is composed of forests, parks, gardens, rivers, canals and lakes. Conference Dates & Venue August, 2018 Berlin, Germany Contact alice@pharmacologyconference.org contact@pharmacologyconference.org Phone: