Name: Essentials of European Medical Device Regulations
Price: 10.99 GBP
Availability: InStock

michor consulting

From conception and strategy to post market maintenance - we advise, accompany, support and train your professionals in all key areas of regulatory affairs, compliance, business organization, quality assurance , risk and interim management in the pharmaceutical, food supplement and medical device industry.

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zenosis

Dundee

We specialise in Pharmaceutical & Biotech courses for healthcare professionals, as well as a suite of essential courses for regulatory and statutory business compliance. As a member of the CPD, you can be assured that our courses meet exacting standards and deliver a compelling training solution. Our courses are consumed by employees at industry leaders such as Merck, Armiral, J&J, Incyte and Boehringer-Ingelheim and Iconplc. Compliance with regulatory requirements is essential for success in any heavily regulated sector, and the Zenosis® range of eLearning provides readily accessible, continually updated courses that enable people to meet the demands placed on them by a vast range of legal statutes, regulatory guidelines, and industrial or professional codes of practice. Zenosis® eLearning provides vital knowledge that will enable your staff to comply with regulatory requirements and increase knowledge and productivity across a wide range of subject areas, such as Drug Safety and Pharmacovigilance, Clinical Trials, Good Manufacturing and Laboratory Processes, Validation and Sales & Marketing in Europe, USA and other regions.

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european centre for clinical research training (eccrt)

Brussels

Training programmes related to clinical research, quality assurance, regulatory affairs, as well as soft skills needed to excel in your job. All these programmes are globally recognised and offer participants a learning journey, with course materials throughout and a comprehension assessment at the end. Our courses are planned as classrooms, live webinars and eLearning & microLearning, or a blend thereof.

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ivdeology

Chatham

We are a growing business of like-minded, friendly professionals who are passionate about Regulatory affairs specifically within the in vitro diagnostic medical device industry. Our aim is to develop our successful team with focus on flexibility, personal development and gender equality. We believe that supporting our staff and helping them grow with us will benefit not only us, but also our customers.

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pharmaeducare

We provide online training and workshops based on various key domains such as Clinical Data Management, Clinical Research & Clinical Trials, GMP, Medical Coding, Medical Devices, Medical Writing, Pharmacovigilance, QMS, Regulatory Affairs as well as other interpersonal skill development courses prepared by experienced industry experts and healthcare professionals. Our courses grant you a comprehensive overview and training of the various fields and processes practised in the pharma-biotech industry. The up-to-date nature of our content and unique teaching style offers you a world-class training experience and a competitive edge in your career.

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nextfairs for exhibitions and conferences

NEXTFAIRS IS A MULTI-FORMAT EVENTS ORGANIZER IN A DIVERSE ARRAY OF INDUSTRIES. WE ARE A FULL-SERVICE PROVIDER OF UNIQUE HYBRID AND VIRTUAL PROGRAMS, B2B & B2C EXHIBITIONS & CONFERENCES THROUGH ITS EXPERTISE, QUALIFIED PERSONNEL, AND REPUTATION, NEXTFAIRS HAS DEVELOPED A UNIQUE BUSINESS PHILOSOPHY THAT ALLOWS IT TO CREATE ROBUST RELATIONSHIPS WITH ITS CLIENTS. We strive to operate as a business solutions integrator by providing full-service management of regulatory affairs, event organizers, and venue management. NeXTfairs seeks to provide value-added services that helps businesses to grow exponentially and enhances their business processes.

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qrec clinical research institute

KaviKamal Group is a enterprise headquartered in Jaipur, Rajasthan, India, comprises of companies operating in Medical Research, Food processing, Education and Social service. Group operates with a mission and objective of serving humanity with Quality services and products to gain leadership with trust. QREC Clinical Research LLP is registered under Ministry of Corporate Affairs (Govt.) having Identification number AAC-3934 and StartupIndia (Govt.) DIPP - 22363. We are CRO providing Clinical Trials (Phase 3 &4), Medical Writing, Medico Marketing, Regulatory Affairs, Clinical Data Management and Statistical Analysis services to complete Pharmaceutical and Healthcare Industry in India and other countries.

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prescription pharma support

Over the last 17 years, Prescription Pharma Support Pvt. Ltd. is globally recognized as a Pharmaceutical Solutions Provider, specializing in Technical Consulting, Recruitment, Training and Sourcing Solutions to the Pharma and Biotech industry, with operations in several countries worldwide. PPS strength lies in our Talent Pool of Global Experts in specific fields - Manufacturing Operations, Quality and Regulatory Affairs, and Research & Development. PPS Experts have hands-on experience in their specific fields and will give you practical Solutions hand-holding you through your specific situations. PPS Specialises in Training Workshops, Corporate Cross-country Recruitments, Technical Consulting and Strategic Sourcing of Products, all focused on the Pharma and Biotech industry. Founded by three entrepreneurs, Asha Shetty, Karen Carvalho & Nikhil Nagri, we at Prescription Pharma Support Pvt. Ltd. (PPS) realize the importance of continuous knowledge as being crucial to the driving force behind any Pharma or biotech Company that needs a global advantage.

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educareglobus

Nagpur

PharmaEducare is dedicated to bridging the knowledge and experience gap between Academia and Industry. We ensure that our students are Industry-ready to take on challenges at Pharmaceutical, Bio-Pharmaceutical, Hospital, Consultancy, and Clinical Research Organizations. We provide online training and workshops based on various key domains such as Clinical Data Management, Clinical Research & Clinical Trials, GMP, Medical Coding, Medical Devices, Medical Writing, Pharmacovigilance, QMS, Regulatory Affairs as well as other interpersonal skill development courses prepared by experienced industry experts and healthcare professionals. Our courses grant you a comprehensive overview and training in the various fields and processes practiced in the pharma-biotech industry. The up-to-date nature of our content and unique teaching style offers you a world-class training experience and a competitive edge in your career. Our pharma training and workshops comprise theoretical and practical aspects of subjects, soft skills required, and pre-recruitment processes. They help you gain expertise and experience and automatically fill the gap between Academia and Industry. Our courses are CPD certified and aim to deliver the most effective and practical learning experience and make you industry-ready.

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personal care regulatory ltd.

Personal Care Regulatory (PCR) are a friendly team of 'in house' cosmetics regulatory, toxicology, compliance and quality experts, offering a comprehensive range of services backed up by the latest safety software and an extensive database of detailed toxicological profiles. It might seem tempting to turn to cheap solutions to 'get the job done' as quickly as possibly. At PCR, it’s more than just paperwork and box ticking. It's about understanding what your business needs and delivering it brilliantly. This is a regulatory company with a difference; experts in compliance across the supply chain. From trademark in-house safety assessment software which enables a faster and more detailed CPSR, bespoke end-to-end compliance service, through to expert label copywriting service, we offer a full range of high quality services and ‘wrap around’ solutions, tailored to growing beauty brands. PCR’s mission and purpose At PCR, we believe that regulation and compliance are the cornerstones of product quality. Our mission is to cut through the complexity of compliance, and offer the level of service and expertise usually reserved for big corporations to growing brands, at a fraction of the cost. We work in partnership with you, acting as your ‘in house’ experts, giving you the confidence to take your brand to the next level. The highest standards, delivered by a team of supportive experts. Above all, we strive to make the process as straightforward as possible, at great value, every time. Dr. Mojgan Moddaresi (Founder) – Personal Care Regulatory About the founder Dr Mojgan Moddaresi (AKA ‘Dr M’) has over 20 years of experience in the pharmaceutical, biopharma and cosmetics industries. She is a pharmacist in training (PharmD) and proudly holds the accolade of receiving the first ever phD in Cosmetic Science from the London College of Fashion in collaboration with Kings’ College, London. Dr M has built on her scientific training and background with extensive experience working with a range of brands. This has led to a unique approach in helping brands to grow and thrive, by giving them access to help and support usually only reserved for larger businesses. Knowing that great compliance and quality support helps a brand to grow faster without hiccups or headaches, she identified one key insight. The best support is usually delivered by a large ‘in house’ team of toxicology, claims and regulatory experts. Smaller brands had previously had to rely on patchy consultation or manufacturer services, and the idea for PCR was born. A comprehensive compliance company which used the latest in data and IT to support a team of experts, offering end-to-end support for growing brands. She still believes that good compliance across claims, safety and quality are the foundations of a strong and differentiated brand. Dr M and her team have a shared passion for product safety, and delivering a service that gives peace of mind to ambitious brands.

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