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We are pleased to announce the first edition of AMWC Asia, held alongside the 6th edition of the Taiwan Dermatology Aesthetics Conference, taking place
4-5-6 May 2018 in Taipei Taiwan.
EuroMediCom...
Concerned sectors: Biology -Biotechnology -Surgery -Oral Surgery -Plastic surgery -Dermatology -Aesthetic Medicine -Physiotherapy -Public Health -
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L’innovation inversée : Une opportunité pour la santé dans le monde
Après six Forums en bilatéral, la Fondation de l’Académie de Médecin...
Concerned sectors: Biomedical -Biotechnology -Surgery -Law and Health -Medical Equipment -Medical Informatics -Emergency Medicine -General Medicine -Forensic Medicine -Public Health -_Other -
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Le 1er Congrès International de Biotechnologie Verte sera organisé par la Faculté Polydisciplinaire de Taroudant en collaboration avec l’Association Ibn Zohr pour la Recherc...
Concerned sectors: Biomedical -Biotechnology -
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journnes sur les techniques eletrophysiologiques et le sommeil...
Concerned sectors: Anesthesia / Resuscitation -Biomedical -Biotechnology -Diabetology -Medical Equipment -Hypnotherapy -Kinesitherapy -Forensic Medicine -Neurosurgery -Neurology -Otorhinolaryngology -
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Course "A Risk Based Approach To IT Infrastructure & Cloud Qualification, Compliance & Control" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant&#...
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Course "Clinical Data Management" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
When new dr...
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Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full...
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Course "The New EU Medical Device regulation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview...
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The Multilateral Initiative on Malaria (MIM) was established in 1997 with a mission to strengthen and sustain through collaborative research and training, the capacity of malaria-endemic countries in ...
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The 5th Microbiome R&D and Business Collaboration Forum: Europe is set to take place on 21 – 22 March in Rotterdam, The Netherlands. Designed with scientists, researchers and businesses in m...
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The 2nd Probiotics Congress: Europe is set to take place on 21 – 22 March in Rotterdam, The Netherlands. Designed with scientists, researchers and businesses in mind, this meeting focuses on ide...
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Overview:
You'll learn how to identify, segregate, control, and disposition non-conforming material. You'll learn about conducting failure investigations and requirements for correction and c...
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This two-day conference will facilitate collaboration between senior representatives from industry, hospitals, universities and regulators.
Extended networking time and small group roundtable discu...
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13th Annual Biomarkers Congress
15-16 February 2018, Manchester, UK
Over 300 delegates representing leading biotech companies, global pharma organisations and internationally renowned academic ins...
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Overview:
It will also consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, as well as the two different device classification s...
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Overview:
This course is NOT a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.
Why should you Attend:
Testing software to prove th...
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Overview:
In this valuable presentation, Excel expert David Ringstrom, CPA, explains how the Office 365 version of Excel 2016 differs from previous versions and perpetual licensed versions of E...
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Overview:
How it may be integrated with the recommendations of the guidance documents on CMC requirements.
Areas Covered in the Session:
Discussion of the elements found in the guidance document ...
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Overview:
Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations.
Why should you Attend:
Expectations for mean...
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Overview:
This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructur...
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Overview:
Companies engaged in the conduct of human clinical trials must adhere to specific government regulatory requirements.Certain documents, content and images related to a clinical trial ...
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Overview:
This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program.
Why s...
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Overview:
Electronic medical records and electronic handling of study data is increasingly common. To involve computer systems in clinical research implies knowledge of 21 CFR Part 11.
Why s...
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