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Compliance4All

161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA.
94539 Fremont
California, États-Unis
Tél : +1 18004479407
Fax : +1 302-288-6884
Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. .

Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.

Thématique :
Pharmacie


Mots clés :
professional education provider, regulatory compliance training, regulatory and compliance training, regulatory trainings, in-person seminars, consulting, learning facility, continuing professional education

Evènements à venir


21 CFR Part 11 Guidance for Electronic Records - 2018

Réf: 26779 Jeudi 21 Juin 2018 - En ligne

ER/ES capability can vary, and the approach should be based on the specific case and the risk of failing to meet the guidance associated with it.

Formation: Pharmacie, Bio-Technologies, Informatique, Management

Controls Over Transportation of Fresh Organic Foods

Réf: 26951 Mardi 26 Juin 2018 - En ligne

The US Department of Agriculture reports punishable fines up to $11,000 and encourages reporting
complaints.

Formation: Médecine, Informatique, Médecine générale, Management, Sécurité sociale, Pour le public

Evènements passés


What are the principles of HEPA filtration?

Réf: 26950 Mardi 12 Juin 2018 - En ligne

This webinar first details and explains the various US and international regulatory requirements
for various clean room classifications.

Formation: Médecine, Informatique, Médecine générale, Management, Sécurité sociale, Pharmacie, Pour le public

How an Organization can remain Compliant with these Regulations

Réf: 26949 Lundi 11 Juin 2018 - En ligne

How an organization can remain compliant with these regulations in their day-to-day operations.

Formation: Médecine, Bio-Technologies, Médecine générale, Management, Sécurité sociale, Pharmacie, Pour le public

What Sponsors Expect and How to Meet their Expectations

Réf: 26947 Vendredi 08 Juin 2018 - En ligne

How to Meet their Expectations, Also learn Managing and avoiding common pitfalls with CROs/Vendors.

Formation: Médecine, Médecine générale, Médecine interne, Management, Sécurité sociale

Which data and systems are subject to 21 CFR Part 11

Réf: 26948 Vendredi 08 Juin 2018 - En ligne

This webinar demystifies Part 11, and get you on the right track for using electronic records
and signatures to greatly increase productivity.

Formation: Médecine, Bio-Technologies, Médecine générale, Management, Sécurité sociale

Why Organizations need to use CAPA, What is its Purpose?

Réf: 26945 Jeudi 07 Juin 2018 - En ligne

Learn how FDA investigates CAPA in organizations, and be prepared for an audit in your organization.

Formation: Médecine, Bio-Technologies, Management, Sécurité sociale

How to Conduct Effective Close out Meetings

Réf: 26946 Jeudi 07 Juin 2018 - En ligne

This webinar is designed to provide the participants a working knowledge of supplier audits.

Formation: Médecine, Bio-Technologies, Sécurité sociale, Management, Pharmacie

Essential Training for IRB Members and Staff

Réf: 26943 Mardi 05 Juin 2018 - En ligne

This webinar serves will provide substantive training of the criteria for IRB approval for new IRB
members/staff who have less than three years of experience.

Formation: Pharmacie, Bio-Technologies, Management, Sécurité sociale

Label Promotion of Drugs and Medical Devices 2018

Réf: 26944 Mardi 05 Juin 2018 - En ligne

This session sets the context for the off-label promotion of medical products starting
with early history and moving to the most recent history of FDA's decision on guidance documents.

Formation: Bio-Technologies, Médecine générale, Management, Sécurité sociale

Drug Substances and Drug Products - Specifications

Réf: 26778 Mercredi 23 Mai 2018 - En ligne

Learn requirements for changing specifiations through the lifestyle of the product.

Formation: Médecine, Pharmacie, Bio-Technologies, Sécurité sociale, Management

Investigator Reporting Responsibilities - OHRP

Réf: 26776 Vendredi 18 Mai 2018 - En ligne

A comparison will be provided for the AE reporting requirements for drugs and devices.

Formation: Pharmacie, Bio-Technologies, Management

Manufacturing Safety - What you don't Know can Harm you

Réf: 26777 Vendredi 18 Mai 2018 - En ligne

In this webinar, we will explore the hazards related to the manufacturing facility on many fronts.

Formation: Pharmacie, Bio-Technologies, Informatique, Management, Sécurité sociale

C-TPAT - Trade Partnership Against Terrorism 2018

Réf: 26775 Lundi 14 Mai 2018 - En ligne

How to develop a standard approach to complying with the voluntary C-TPAT guidelines, and Strategies for reducing the cost and complexity of compliance with C-TPAT.

Formation: Pharmacie, Bio-Technologies, Management, Sécurité sociale

Fundamentals of Risk Management in Clinical Research 2018

Réf: 26774 Vendredi 04 Mai 2018 - En ligne

Practical aspects of developing key performance and quality indicators at all stages of clinical trials will be discussed.

Formation: Pharmacie, Management, Sécurité sociale

How to Comply with 21 CFR 11 Requirements

Réf: 26773 Mercredi 02 Mai 2018 - En ligne

What are future expectations for EMRs (FDA Draft Guidance) and the impact on sponsors and sites.

Formation: Pharmacie, Management, Sécurité sociale

Label Promotion of Drugs and Medical Devices

Réf: 26604 Mardi 24 Avril 2018 - En ligne

Overview: This session sets the context for the off-label promotion of medical    products starting with early history and moving to the most recent history    of FDA's decision on guidance documents.   Why should you Attend: This class presents the latest ...

Formation: Pharmacie, Pour le public

How a Quality and Lean Steering Committee can be Effectively Utilized

Réf: 26603 Vendredi 20 Avril 2018 - En ligne

How a quality and lean steering committee can be effectively utilized in any type of organization.

Formation: Pharmacie, Pour le public

Failure Modes - How to use these Kinds of Methods Together

Réf: 26601 Mercredi 18 Avril 2018 - En ligne

This presentation provides you with the information you need to for effective FMEA use

Formation: Pharmacie, Médecine, Pour le public

ISO 62366 - How to Conduct a Human Factors

Réf: 26602 Mercredi 18 Avril 2018 - En ligne

This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/usability validation.

Formation: Médecine, Pharmacie, Pour le public

Understanding and Meeting your Regulatory & Processing Responsibilities

Réf: 26600 Lundi 16 Avril 2018 - En ligne

How DMFs fit into FDA's regulatory processes for review of drug and biologic applications.

Formation: Pharmacie, Médecine, Pour le public

Best Practices for Foundational Employee Success 2018

Réf: 26599 Mercredi 11 Avril 2018 - En ligne

Learn to interact with Human Resources to create a coordinated onboarding strategy

Formation: Pharmacie, Pour le public

ISO 13485 & ISO 9001 - How to Choose Which One to Implement

Réf: 26598 Mardi 10 Avril 2018 - En ligne

Attending this webinar will provide information to help organizations make the best decisions for their business.

Formation: Pharmacie, Médecine, Pour le public

Medical Device Single Audit Program Preparation

Réf: 26595 Vendredi 06 Avril 2018 - En ligne

Overview: The International Medical Device Regulators Forum (IMDRF) recognizes    that a global approach to auditing and monitoring the manufacturing of    medical devices could improve their safety and oversight on an    international ...

Formation: Médecine, Pharmacie, Management

Quality Audit According to Gxp-GMP Requirements 2018

Réf: 26596 Vendredi 06 Avril 2018 - En ligne

Overview: GMP regulations describe required quality management system for    production and testing of products in these regulated industries. The    purpose of the GMP regulations is to ensure that a product is safe and    meets its intended ...

Formation: Médecine, Pour le public