Congrès dentaire - Formation dentaire

Good Documentation Guideline (Chapter <1029> USP)

Réf: 30382 Jeudi 24 Octobre 2019 - Palo Alto ^US

Editorial This webinar will familiarize participants with USP Chapter <1029> on good documentation guidelines. This session will wrap up the general concept and will provide information as to what needs to be documented in certain records.
  Objectives Good Documentation ...

Data Integrity and Privacy: Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

Réf: 30703 Mardi 05 Novembre 2019 - Palo Alto ^US

Editorial This 21 CFR Part 11 compliance training will guide you through the requirements of Part 11 and will also explain its 3 primary areas: SOPs, product features and validation (10 step risk based approach).
  Objectives This webinar describes exactly what is required for ...

Basic Clean Room Technology, Operation and Contamination Control in a Nutshell

Réf: 30347 Jeudi 07 Novembre 2019 - Palo Alto ^US

Editorial Attend this webinar to understand the Clean Room regulations, design, classification, sources and types of particles. Learn how to create a common ground between these varying regulations and requirements. It will discuss the types of micro-organisms, routine monitoring processes, and ...

Basic Clean Room Technology, Operation and Contamination Control in a Nutshell

Réf: 30707 Jeudi 07 Novembre 2019 - Palo Alto ^US

Editorial Attend this webinar to understand the Clean Room regulations, design, classification, sources and types of particles. Learn how to create a common ground between these varying regulations and requirements. It will discuss the types of micro-organisms, routine monitoring processes, and ...

11th Dental Facial Cosmetic Conference & Exhibition

Réf: 28584 08/11/2019 -> 09/11/2019 - Dubai ^AE

Aesthetic Dentistry

No Limit

Réf: 28944 Vendredi 08 Novembre 2019 - Charleroi ^BE

Editorial Entrez votre message d'accueil pour présenter brièvement votre évènement.
  Programme Dr Henri Diederich Dr Federico Maschio & Dr Patrice Marie Lejuste Mr Jérôme Lasserre & Mr Andrej Djurkin    Comité d'organisation ...

Aseptic Processing Overview and Validation

Réf: 30708 Lundi 11 Novembre 2019 - Palo Alto ^US

Editorial This course will provide an overview of the requirements for aseptic and bulk manufacturing operations, including facility design, contamination controls and acceptable personnel behaviors. Objectives At the completion of this course, attendees will be able to: Explain the ...

How to Conduct Annual Product Reviews to Achieve GMP Compliance Annual

Réf: 30709 Mardi 12 Novembre 2019 - Palo Alto ^US

Editorial This webinar will give a brief overview of the general procedure for the preparation and documentation of the Annual Product Quality Review and also focuses on the regulations and the regulatory requirements as per US and Europe.
  Objectives This webinar will ...

Writing and Revising SOPs for Increased Operational Efficiency

Réf: 30711 Mardi 12 Novembre 2019 - Palo Alto ^US

Editorial This webinar will discuss how to more effectively write and revise standard operating procedures (SOPs) with a focus on increasing operational efficiencies.
  Objectives What is an SOP? Ways to structure systems of SOPs Examples of sections to include in an ...

Conducting Successful FDA Meetings

Réf: 30712 Vendredi 15 Novembre 2019 - Palo Alto ^US

Editorial If you develop or manufacture a product regulated by FDA you will need to interact with FDA employees. Knowing what makes FDA employees the way they are, will help immensely in understanding how to deal with FDA.
  Objectives Become familiar the types of jobs within FDA ...

2019 – 23rd International Conference on Research in Life-Sciences & Healthcare (ICRLSH), 16-17 November, Singapore

Réf: 29642 16/11/2019 -> 17/11/2019 - Singapore ^IN

ICRLSH

7th Annual Congress on Dental Medicine and Orthodontics

Réf: 28806 18/11/2019 -> 19/11/2019 - Indonesia ^ID

Dental Conferences, Dentists congress, Dental implant conferences, Emergency Dental Care events, Endodontic and Orthodontic conferences, Oral health events, Oral Surgery meetings, Clinical Dentistry Conferences, Dental care Congress, Bali 2019

How to Prepare a Standard Operating Procedure (SOP)?

Réf: 30383 Mardi 19 Novembre 2019 - Palo Alto ^US

Editorial This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review and revise SOPs and maintain compliance over the course of the SOP life-time.
  Objectives Standard Operating Procedures ...

How to Prepare a Standard Operating Procedure (SOP)?

Réf: 30713 Mardi 19 Novembre 2019 - Palo Alto ^US

Editorial This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review and revise SOPs and maintain compliance over the course of the SOP life-time. Objectives Record compliance with examples What ...

Best Practices for an Effective Cleaning Validation Program

Réf: 30715 Mardi 19 Novembre 2019 - Palo Alto ^US

Editorial This training program will be beneficial to personnel directly involved in the development of cleaning procedures, cleaning validation programs and plans. Additionally, those responsible for cleaning validation protocols and execution activities, including validation and laboratory ...

Complaint Handling Requirements (US); Interrelationship with CAPA, Change Control, Adverse Event Reporting, Recalls and Life Cycle Process ...

Réf: 30716 Mardi 19 Novembre 2019 - Palo Alto ^US

Editorial This training program will provide the regulatory requirements (US) for complaint handling in the medical device and pharmaceutical industries. The course will touch on complaint sources, and details will be furnished on the interrelationships regarding complaint handling/change ...

Validation Master Plan - The Unwritten Requirements

Réf: 30385 Mercredi 20 Novembre 2019 - Palo Alto ^US

Editorial This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a company's ...

Validation Master Plan - The Unwritten Requirements

Réf: 30717 Mercredi 20 Novembre 2019 - Palo Alto ^US

Editorial This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a company's ...

GxP/GMP Requirements and its Consequences for Documentation and Information Technology Systems

Réf: 30718 Mercredi 20 Novembre 2019 - Palo Alto ^US

Editorial Attend this webinar to learn the connection between GxP/GMP with document control and IT systems. Attendees will learn how to manage control documents to pass quality audit and information technology systems in compliance with GxP/GMP ...

What else ?

Réf: 28946 Samedi 23 Novembre 2019 - Liège ^BE

Editorial Entrez votre message d'accueil pour présenter brièvement votre évènement.
  Intervenants Marie-cécile manière – France Les anomalies de l’émail, traitez-les! Renaud Noharet – France Comprendre la biologie et les outils digitaux pour une implantologie ...

How to Achieve a Compliant and Effective Cleanroom Design and Facility Validation

Réf: 30756 Lundi 25 Novembre 2019 - Palo Alto ^US

Editorial This training program will discuss designing an effective cleanroom facility validation protocol and report, when and how to transition into the routine environmental monitoring processes, how to maintain a state of control within the cleanroom, and the routine environmental ...

4-Hr Virtual Training: How to Respond to an FDA Investigation

Réf: 30386 Mercredi 04 Décembre 2019 - Palo Alto ^US

Editorial This FDA investigation training program will deconstruct best practices for handling unannounced FDA visits, responding to a 483 or a warning letter, and the effect of an FDA investigation. The program will also discuss basic concepts that should be employed by everyone regulated by ...

4-Hr Virtual Training: How to Respond to an FDA Investigation

Réf: 30726 Mercredi 04 Décembre 2019 - Palo Alto ^US

Editorial This FDA investigation training program will deconstruct best practices for handling unannounced FDA visits, responding to a 483 or a warning letter, and the effect of an FDA investigation. The program will also discuss basic concepts that should be employed by everyone regulated by ...

Human Error Reduction Techniques for Floor Supervisors

Réf: 30728 Jeudi 05 Décembre 2019 - Palo Alto ^US

Editorial Attend this course to gain practical approaches for supervision on the floor, strategies to get your group in sync and approach issues in GMP related environments by using a specific methodology to correct, prevent and avoid re-occurrence of these ...

Overcoming Obstacles of The Canadian Drug Regulatory Landscape

Réf: 30729 Jeudi 05 Décembre 2019 - Palo Alto ^US

Editorial The Canadian Drug Approval Process is misunderstood by many and considered harsh by some. We will explore reasons why the Canadian market should not be overlooked and the benefits of including Canada in strategic drug development initiatives. We will share insights and practical ...