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List of health conferences, educations - cme : upcoming 1805

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Ensuring 21 CFR 11 Compliance at Suppliers

Ref: 20754 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

4th CROWN Congress

Ref: 21011 01/27/2015 -> 01/29/2015 - Philadelphia US

Objectives An ELITE Gathering of Clinical Decision-Makers Learn, Network and Engage on Topics Critical to the Effective Design, Development and Execution of Clinical Trials. Program   The 4th CROWN Congress, taking place January 27-29 in Philadelphia, boasts a newly designed format, ...

Conference & Seminar: Pharmacy

FDA Recordkeeping Requirements

Ref: 21265 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21273 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21274 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21286 Tuesday January 27th, 2015 - Houston US

DESCRIPTION Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered will include: ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21287 Tuesday January 27th, 2015 - Houston US

DESCRIPTION Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you to retain, and ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21309 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21310 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

Software Design for Medical Devices Europe

Ref: 21332 01/27/2015 -> 01/28/2015 - Munich DE

  Finding and maintaining the balance between compliance and the development of medical device software quality and usability whilst being truly agile can be challenging.    The medical device industry is ever changing and evolving, especially in recent years with adjustments ...

Conference & Seminar: Pharmacy

Live webinar Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21341 Tuesday January 27th, 2015 - Houston US

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America.

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21355 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21356 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21369 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21370 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21398 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21399 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21417 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21418 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21434 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21435 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry

Ref: 21470 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Why Should You Attend:    This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered ...

Conference & Seminar: Medicine

FDA Recordkeeping Requirements

Ref: 21471 Tuesday January 27th, 2015 - Houston US

DESCRIPTION     Learn the SOPs and policies to have, how to incorporate risk assessments, how to ensure each of your SOPs generate clear records as proof of compliance, and get the details of an effective FDA recordkeeping program. Learn the types of documents FDA expects you ...

Conference & Seminar: Medicine

21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

Ref: 21266 Wednesday January 28th, 2015 - Houston US

DESCRIPTION     All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records.  Medical device manufacturing plants, required to follow ...

Conference & Seminar: Medicine

21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

Ref: 21275 Wednesday January 28th, 2015 - Houston US

DESCRIPTION     All life science businesses are required to maintain their Quality Management System (QMS) processes in a state of control, via controlled documents and objective evidence in the form of records.  Medical device manufacturing plants, required to follow ...

Conference & Seminar: Medicine

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