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List of medical conferences and educations - cme in Palo Alto : 31 results

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The Most Serious FDA 483s - How to Avoid Them

Ref: 28981 Tuesday March 12th, 2019 - Palo Alto US

Editorial This webinar on avoiding serious FDA 483s will explain FDA's changed audit focus based on recent top 483 findings and provide practical tips on how to better prepare your company's internal audit program to avoid serious Form 483 observations.  Objectives Recent FDA audits ...

Conference & Seminar: Management

CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers

Ref: 28982 Tuesday March 12th, 2019 - Palo Alto US

Editorial This webinar will include a detailed discussion of Contract Manufacturing Organizations (CMO) Quality Agreement topics such as change control, documentation, facilities and equipment, lab controls, sub-contracting, etc. Attendees will learn how to comply with new FDA and EU guidelines ...

Conference & Seminar: Management

FDA Regulations for Marketing OTC Drugs in the U.S.

Ref: 28983 Thursday March 14th, 2019 - Palo Alto US

Editorial This training program will illustrate why it’s essential to understand FDA regulations and OTC labeling requirements to market OTC drugs in the U.S. Objectives Understanding U.S. FDA regulations and the OTC monograph system and its labeling requirements will help companies assure ...

Conference & Seminar: Management

Integrating Case Management Across the Continuum of Care: Managing Cost and Length of Stay

Ref: 28984 Monday March 18th, 2019 - Palo Alto US

Editorial In this webinar you will learn how to integrate case management across the continuum in reducing your hospital’s cost and length of stay. You will learn how to coordinate the patient’s transition between healthcare systems and settings such as moving from the hospital to ...

Conference & Seminar: Management

ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements?

Ref: 28985 Tuesday April 02nd, 2019 - Palo Alto US

Editorial This webinar will benefit medical device companies planning to have a CE mark under the European Union Directive 93/42/EEC. We will discuss what is new in ISO 14971:2012 and help you avoid delays in obtaining or maintaining your CE mark for compliance to the Medical device Directive, ...

Conference & Seminar: Management, Hospital

Reprocessing Reusable Medical Devices - Cleaning and Labeling Requirements

Ref: 28939 Thursday April 11th, 2019 - Palo Alto US

Editorial This training program will explain the rationale, the legal requirements and some methods commonly used for reprocessing and validating reusable medical devices. Program Any firm reprocessing another manufacturer's medical device becomes the legal manufacturer with all the ...

Conference & Seminar: Hospital, Management

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