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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.

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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

Excel - Workbooks and FDA Device Regulations

Réf: 26436 Mercredi 21 Mars 2018 - En ligne

Learn methods to recognize the use of Excel workbooks in production or the quality system.

Formation: Pharmacie, Médecine, Santé Publique

GMP for Phase I Investigational Drug Products 2018

Réf: 26437 Jeudi 22 Mars 2018 - En ligne

The necessary content of the IND will not be discussed in this webinar, but the specific GMPs for Phase I Investigational drugs will be understood by attendees.

Formation: Médecine, Pharmacie

European Data Protection Regulation - 2018 Implementation

Réf: 26438 Jeudi 29 Mars 2018 - En ligne

Individuals in the EU may be unwilling to transfer personal data outside the EU if they are uncertain about the level of protection in other countries. How US businesses need to pay attention to this impact will be addressed.

Formation: Médecine, Santé Publique, Pharmacie

How to Identify the Causes Behind the Autism Spectrum Disorder

Réf: 26439 Vendredi 30 Mars 2018 - En ligne

The discussion takes the participants through how DMAIC was successfully used to make viable differences with live metrics and results.

Formation: Médecine, Santé Publique, Management, Pharmacie

Discussion on Raw Material Methods and Specifications

Réf: 26593 Mercredi 04 Avril 2018 - En ligne

The quantities and quality of each inactive ingredient is critical to the function and design of the final product formulation.

Formation: Pharmacie, Médecine, Management

Validation for the New FDA Inspections

Réf: 26594 Jeudi 05 Avril 2018 - En ligne

How to conduct a software validation program that will satisfy FDA requirements and produce a safe product.

Formation: Pharmacie, Médecine, Management, Toxicologie

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

Compliance for Electronic Records and Signatures 2018

Réf: 26597 Vendredi 06 Avril 2018 - En ligne

Overview: This webinar demystifies Part 11, and get you on the right track for using    electronic records and signatures to greatly increase productivity.   Areas Covered in the Session: Which data and systems are subject to Part 11 What Part 11 means to you, not ...

Formation: Médecine, 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

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

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

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

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

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 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

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

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

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

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

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

Evènements passés

Dietary Supplements CGMPS - 21 CFR 111 Compliance 2018

Réf: 26434 Mercredi 14 Mars 2018 - En ligne

This is to ensure the quality of the dietary supplement and to ensure that the dietary supplement is packaged and labeled as specified in the master manufacturing record.

Formation: Médecine, Pharmacie

Write an Effective Standard Operating Procedure

Réf: 26435 Mercredi 14 Mars 2018 - En ligne

This webinar will instruct the participant on how to write, organize, and maintain SOPs and train personnel in a way that will ensure compliance in a way that is concise, reproducible and easy to follow.

Formation: Médecine, Santé Publique, Pharmacie