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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


Evènements passés


FDA Inspections: From SOP to 483 in (2019)

Réf: 29658 Vendredi 28 Juin 2019 - En ligne

Overview: Does the FDA call in advance or just show up at my door? Where do I let the inspector go? Do I give them a tour? What should I let them see? Who should I let them talk to? Are they ever going to leave?   Why should you Attend: This session will discuss how to prepare for ...

Formation: Médecine, Bio-Technologies, Santé Publique, Pharmacie

Investigation and Root Cause Analysis to Meet FDA Expectations

Réf: 29657 Mercredi 26 Juin 2019 - En ligne

Overview: This live interactive presentation will also discuss the regulations associated with the detection, correction and prevention of human errors in GMP manufacturing and laboratory processes.   Why should you Attend: We will focus on improved techniques to get to the real ...

Formation: Acupuncture, Médecine

21 CFR Part 11 - Compliance for Electronic Records and Signatures

Réf: 29997 Mercredi 26 Juin 2019 - En ligne

This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and
how conformance to Part 11 differs from just having good IT security.

Formation: Médecine, Bio-Technologies, Management, Santé Publique

Responsibility for Off-label Claims in Social Media

Réf: 29655 Mardi 25 Juin 2019 - En ligne

Overview: One big issue is how you patrol and control what someone else is saying about your product in a public forum. Once the off-label information is out there, what is scope your responsibility?   Why should you Attend: What is considered "off-label" Using social media website ...

Formation: Médecine, Bio-Technologies, Pharmacie

Canadian Drug and Health Products Regulatory Landscape

Réf: 29656 Mardi 25 Juin 2019 - En ligne

Overview: The focus will be on drugs, biologics and medical devices, We will also be providing an overview of how the regulatory landscape is currently evolving for most efficient strategic planning.   Why should you Attend: This webinar will give you a snap shot of what is current, ...

Formation: Médecine, Bio-Technologies

Excel Spreadsheet Validation for FDA 21 CFR Part 11 (2019)

Réf: 29654 Vendredi 21 Juin 2019 - En ligne

Overview: These may be used for GxP regulated activities, and they present particular compliance challenges, as Excel and other spreadsheets are not originally designed for the regulated environment.   Why should you Attend: Part 11 / Annex 11 Computer Systems Validation (CSV) is to ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique

ISO/IEC 17025:2017 Section 7 - Process Requirements and Section 8

Réf: 29652 Jeudi 20 Juin 2019 - En ligne

Overview: How does the new standard impact laboratories that are already accredited and how do you ensure staff adherence and ongoing compliance to minimize corrective actions arising from accreditation audits?   Why should you Attend: What are the changes to the technical and ...

Formation: Médecine, Bio-Technologies, Pharmacie

Auditing Laboratories Conducting Assays Supporting Biologics

Réf: 29653 Jeudi 20 Juin 2019 - En ligne

Overview: Sponsors or consultants auditing labs on behalf of a pharmaceutical or biopharmaceutical company need strong tools for preparing and conducting audits.Careful consideration of the work that will be performed at the laboratory provides a working framework for the content of the ...

Formation: Médecine, Pharmacie, Bio-Technologies, Santé Publique

Latest Master Validation Plan - The Unwritten Requirements

Réf: 29651 Mardi 18 Juin 2019 - En ligne

Overview: FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies. One major failing is lack of sufficient or targeted risk-based company-wide V&V planning.   Why should you Attend: Verification and validation requirements have ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique

Food Business!! - Business Continuity & Disaster Recovery

Réf: 29650 Mercredi 12 Juin 2019 - En ligne

Overview: This course will outline the issues that need to be considered in the preparing to respond to disasters, and will suggest ways to minimize impact to the business and to maintain consumer safety.   Why should you Attend: Consumer Safety is paramount in the food industry, ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique

How to Analyze Financial Statements 2019

Réf: 29649 Lundi 10 Juin 2019 - En ligne

Overview: Grab a cup of coffee and join us to learn how to analyze the numbers, and use this intel to juice up virtually every facet of your organization's operations from marketing, to finance, to HR, to customer service and sales.   Why should you Attend: Accounting and finance is ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique

Good Documentation Guideline (Chapter 1029 USP)

Réf: 29659 Lundi 10 Juin 2019 - En ligne

Overview: This 60-min 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.   Why should you ...

Formation: Médecine, Bio-Technologies, Santé Publique, Pharmacie

When Conducting cGMP Regulatory Inspections 2019

Réf: 29648 Vendredi 07 Juin 2019 - En ligne

Overview: Yet GMPs have been enshrined into law for many countries and a drug/biologic/medical device manufacturer should have a reasonable expectation of all inspections being the same.   Why should you Attend: This webinar will cover the key areas of how ICH Q7 was established, ...

Formation: Médecine, Bio-Technologies, Santé Publique

Implementing a Compliant Stability Program for Biologics

Réf: 29647 Mercredi 05 Juin 2019 - En ligne

Overview: Biologics, as well as small molecule pharmaceutical products, require expiry dating.The complex structure of large molecules presents greater opportunities for degradation. Biologics may lose identity by cleavage ultimately resulting in loss of potency.   Why should you ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique

Overcoming Obstacles of the Canadian Drug Regulatory Landscape

Réf: 29283 Mardi 28 Mai 2019 - En ligne

Overview: Through this presentation, you will develop a comprehensive understanding of the Drug Approval Process and in parallel examine major misconceptions and misunderstandings.   Why should you Attend: We will share insights and practical examples that facilitate a positive, ...

Formation: Médecine, Bio-Technologies, Management, Santé Publique, Pharmacie

FDA's Quality Metrics - Latest Advances

Réf: 29281 Vendredi 24 Mai 2019 - En ligne

Overview: This is a very important webinar for the FDA who is planning to use the quality metrics as part of their risk based inspection process.   Why should you Attend: This is a very important initiative for the FDA who is planning to use the quality metrics as part of their risk ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique, Toxicologie

How to conduct a Compliance Gap Analysis for ERM

Réf: 29282 Vendredi 24 Mai 2019 - En ligne

Overview: This webinar will explain how to conduct a compliance gap analysis for Enterprise Risk Management (ERM). Attendees will learn best practices to ensure ERM compliance.   Why should you Attend: Many companies today are "short staffed" and may skip vital steps that are ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique

How to Create a Medical Software Development File - ISO 62304

Réf: 29280 Lundi 13 Mai 2019 - En ligne

Overview: You will learn, how to apply the ISO 62304 in the medical software development process and how to create a medical software development file.   Why should you Attend: You should attend this webinar to understand, what is the ISO 62304 for medical software and how is the ISO ...

Formation: Pharmacie, Médecine, Bio-Technologies, Management, Santé Publique, Toxicologie

Statistical Hypothesis Tests: Concepts and Applications

Réf: 29277 Mardi 07 Mai 2019 - En ligne

Overview: This training program will cover statistical hypothesis testing concepts including: null and alternate hypotheses, test statistics, p-values, confidence intervals, confidence levels, power, power curves, and sample sizes.   Why should you Attend: This webinar will lay the ...

Formation: Médecine, Bio-Technologies, Santé Publique, Pharmacie

Architect and Implement Solution 2019

Réf: 29279 Mardi 07 Mai 2019 - En ligne

Overview: We will cover how to identify, analyze and document the events and environmental surroundings that can adversely affect the organization.   Why should you Attend: The FFIEC is a wonderful guideline that banks are supposed to follow, but the interpretation of the guideline ...

Formation: Médecine, Bio-Technologies, Toxicologie, Santé Publique

Quality Control for Microbiological Media and Reagents

Réf: 29276 Vendredi 03 Mai 2019 - En ligne

Overview: This webinar will help you develop a quality control program that fits your microbiological laboratory's needs. We will explicitly not cover any serological, immunological or molecular tests.   Why should you Attend: In microbiology laboratories, there are a wide array and ...

Formation: Pharmacie, Médecine, Bio-Technologies, Toxicologie, Santé Publique

Quality Risk Management Overview 2019

Réf: 29275 Jeudi 02 Mai 2019 - En ligne

Overview: Attendees will come away with the ability to recognize the purpose and value of Quality Risk Management QRM. Explain the level of risk based on severity, occurrence, and detectability and how the QRM process is used to make decisions.   Why should you Attend: It can ...

Formation: Médecine, Bio-Technologies, Toxicologie, Santé Publique

Turn a Culture of Quality Into a Competitive Advantage

Réf: 29042 Mardi 23 Avril 2019 - En ligne

Overview: A culture of quality is a powerful tool for creating an effective and    efficient Quality Management System. A culture of quality is not    accidental but can be purposefully nurtured and developed.   Why should you Attend: Every organization ...

Formation: Médecine, Bio-Technologies, Santé Publique, Toxicologie

Controlled Document System for a Life Sciences Manufacturing Plant

Réf: 29041 Jeudi 18 Avril 2019 - En ligne

Overview: Life science manufacturing plants have the additional responsibility    to ensure that each and every step of the manufacturing process is    controlled by work instructions, SOPs, set-up instructions, equipment    maintenance, and support ...

Formation: Pharmacie, Médecine, Bio-Technologies, Santé Publique

How to Implement MDSAP-Requirements into your ISO 13485

Réf: 29040 Lundi 15 Avril 2019 - En ligne

Overview: How a smart implementation of these requirements in the quality    management system is possible and finally how the audit for five    countries (Australia, Brazil, Canada, Japan, US) is working.   Why should you Attend: Your implementation time ...

Formation: Médecine, Bio-Technologies, Toxicologie, Santé Publique, Pharmacie