10th European Congress on Epileptology
The 10th ECE programme will cover cutting-edge research in epilepsy through presentations from leaders in the field, including lectures by world-renowned scientists on topics at the interfaces of epilepsy. The schedule will also feature a coordinated clinical teaching programme. ...
Event at:
ExCeL London
in
London
-
United Kingdom
Type of Event:
Industry Events - Pharmaceutical - Medical
|
International Conference on Central Nervous System - Drugs Effects & Novel Drug Development
Central Nervous System-2012 is a remarkable event which brings together all the leading universities, Central Nervous System researchers as well as institutions, making the conference a perfect platform to share experiences, foster collaborations across industry and academia and also evaluate emerging technologies across the globe. ...
Event at:
Philadelphia, USA.
in
Philadelphia
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies
This FDA Inspection training provides concrete strategies for planning remediation projects.
Why Should You Attend:
Today's manufacturing and quality environments are highly automated and computerized. Manufacturers facing FDA pre-approval inspections (PAI) as well as those who will be re-inspected following inspectional observations (FDA-483), warning letters and other compliance issues ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water
This 6-hr training will focus on important microbial issues with pharmaceutical water systems and provide proven solutions for microbial control. Attendees will learn effective sanitation and validation approaches to successfully control biofilm in water systems.
Why Should You Attend:
This interactive one-day course provides a thorough understanding of what makes water systems have microbial p ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Acceptance Sampling by Variables Using Z1.9
This 90-minute webinar on sampling plans using ANSI/ASQ Z1.9 will explain the methods in Z1.9 and shows how to use it in a more modern setting (using simple statistical calculators).
Why Should You Attend:
Many companies use attribute sampling plans at incoming, in-process, and final inspection. The common approach uses ANSI/ASQ Z1.4. There is an alternate, however, that may reduce cost. Samplin ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
The Autism Show
The national event for autism dedicated to the two million people in the UK who live and work with autism on a daily basis. ...
Event at:
ExCeL London
in
London
-
United Kingdom
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Auditing Systems for 21 CFR Part 11 Compliance: Preparing Yourself for Inspection
This webinar will present a methodology for system assessment, risk-analysis, 21CFR Part 11 compliance, remediation and inventory, along with templates and forms that attendees can modify for their own business.
Why Should You Attend:
Can you show me how you manage your computer systems in compliance with 21CFR Part 11?
This presentation will describe a process which has prepared several ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Global Pharma Manufacturing Summit 2012
Now in its seventh year, the Global Pharma Manufacturing Summit has grown into the premier networking opportunity for industry leaders involved in small molecule and biologic pharma manufacturing. Senior executives and decision-makers from across the pharmaceutical industry will spend two days this June discussing solutions to the universal challenges facing every organization in the current age o ...
Event at:
NJ Expo Centre
in
NJ
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
ICH Q10moving from GMPs to a Pharmaceutical Quality System
This ICH Q10 training /webinar will discuss the evolution and interpretation of the pharmaceutical GMPs as a quality control regulation to the Quality Assurance emphasis of the Pharmaceutical Quality System as defined in ICH Q10.
Since the release of the Quality System Regulation for medical devices, the FDA has been trying to transition the pharmaceutical industry to a Quality System approach t ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Device Corrections and Removals
This 90-minute webinar on device corrections and removals will clarify your obligations for corrections and removals under Part 806 of the FDA regulations.
Why Should You Attend:
If you send a letter to a customer that says, “We found a problem, but, not to worry, we will fix it for you!”, you may have invoked the Corrections and Removals process. Under Part 806 of the FDA regulations, you must ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
21 CFR Part 11 compliance for Electronic Medical Records
This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records.
De_ion:
Electronic Medical Records are the future. Some facilities and doctors are already using this cutting edge technology, and the medical community in general is moving in this direction.
FDA regulations governing electronic records and electronic si ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Pre-Approval Statements and Representations by Pharmaceutical Manufacturers
This 90-minute webinar will help you understand the problems that can occur with statements by pharmaceutical manufacturers directed to off-label uses of pharmaceuticals.
Why Should You Attend:
Off-label uses cannot be legally promoted. Promoting off-label uses may be viewed by FDA as actionable under the False Claims Act. Criminal and civil liabilities can be substantial for manufacturers. One ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Supplier Controls to Meet Tougher U.S. FDA Requirements
This 90-minute webinar on supplier controls will help you refine your supplier management and audits to match the FDA's tougher position. We will evaluate the chief areas of change to see how to better prepare a supplier chain management and audit program.
Recent FDA statements and actions indicate the past ways of managing a company's supply chain / outsourcing will no longer be accepta ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Pharma Outsourcing and Procurement 2012
Pharmaceutical outsourcing is growing exponentially amidst challenging price restrictions, US health care reforms and reduced revenues.
The Pharma Outsourcing and Procurement Summit 2012 addresses the urgent need for pharma to identify and locate the best outsourcing partnerships and solutions to stay competitive in an uncertain climate whilst addressing heightened regulatory pressures and ne ...
Event at:
Hotel Palace Berlin
in
Berlin
-
Germany
Type of Event:
Industry Events - Pharmaceutical - Medical
|
The Allergy and Free From Show
Discover solutions, take control at the Allergy & Free From Show.
The Allergy & Free From Show is the UK’s largest annual gathering of people living with:
allergies _ skin conditions _ eczema
migraines _ coeliac disease _ hay fever _ asthma
food intolerances _ chemical sensitivities
The Allergy & Free From Show is the place where you can start to take control. ...
Event at:
Olympia West Hall
in
London
-
United Kingdom
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Equipment Calibration in FDA QSR – Regulations and Warning Letters
This webinar explains concepts required for a calibration program that satisfies FDA’s Quality System Regulation (QSR), ISO 13485, and ISO 9001. It defines the concepts of accuracy and precision that define the measuring equipment’s requirements. It also explains the meaning of traceability.
Why Should You Attend:
Managing your calibration program is a key element in delivering good products an ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
The Hero of Manufacturing Contamination Control -- The Microbiology Lab
This webinar on Contamination Control will discuss, how the micro lab can be more effectively utilized to prevent or head off microbial contamination issues as well as effectively resolve problems like recurring micro failures, investigations, and ineffective CAPAs.
Why Should You Attend:
The Microbiology Lab must take leadership in contamination control support for production because it is the ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
DEA, Your Registration and How to Lose It
This 2-hr webinar on DEA Due Diligence will cover several recommendations to improve the Corporate Due Diligence when controlled substances and regulated chemicals are purchased by their customers and the steps that can be taken to detect and prevent the illicit use or diversion of any narcotic drug sold to customers.
Understanding the DEA "Know Your Customer Policy" is important and t ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
3-hr Virtual Seminar: FDA Medical Device Regulation for the Beginner
This 3-hr virtual seminar will provide an introduction to FDA’s Regulation of Medical Devices and is intended for the Beginner. It will cover device classification, the device manufacturer’s and/or distributor’s regulatory responsibilities, requirements for labeling and user fees, fda inspections and enforcement.
Why Should You Attend:
This introductory course will present the beginner with an ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
12th Social Study of ICT Conference
12th Social Study of ICT Conference - Health Information Systems: Searching the Past, Finding a Future
Health Information Systems is in transition; money is tight and strategic ambitions are shifting. This conference explores two issues: what lessons can be learned from recent experiences with innovative health information systems and how should we re-shape our commitment to building health inf ...
Event at:
LSE
in
London
-
United Kingdom
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Acceptance Activities in FDA QSR – Regulations and Warning Letters
This webinar will explain the FDA QSR requirements for acceptance activities related to medical device manufacturing. It clarifies FDA’s intent using the preamble to the regulations. We will analyze recent Warning Letters and provide tips to ensure that your acceptance activities fully complies with the regulatory requirements.
Why Should You Attend:
Acceptance activities are common in device m ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Pharmaceutical Water System Use & Monitoring
This webinar on pharmaceutical water systems will explain practical best practices for outlet use and sampling to reflect the true water quality and how to most effectively use the resulting data to improve manufacturing’s water use practices and maintain water system control before problems arise from biofilm-related contamination.
Why Should You Attend:
Problematic removal of pristine water f ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Brain Matters: The divided mind
Iain McGilchrist has had a unique career. He began as a literary academic but then switched to medicine, becoming a neuroimaging researcher at Johns Hopkins Hospital, Baltimore, USA. Then he moved on to psychiatry and, until recently, was a consultant psychiatrist in London. He has been elected to Fellowships of All Souls College, Oxford, and of the Royal College of Psychiatrists. Now he is a full ...
Event at:
Wellcome Collection
in
London
-
United Kingdom
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
This webinar on risk-benefit decisions in medical device manufacturing provides attendees with an understanding of the two recently released FDA draft guidance documents - “Factors to Consider when Making Benefit-Risk Determinations in Medical Device Premarket Review” and “Design Considerations for Pivotal Clinical Investigations for Medical Devices”. It also covers the relationship to regulatory ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Full-day Virtual Seminar: How to Establish A Medical Device Quality System
This 6-hr virtual seminar will present a detailed overview of regulatory requirements necessary for establishing a medical device quality system in the US, which is relevant and applicable for quality system management in global jurisdictions of medical device products.
This 6-hr virtual seminar is intended to demonstrate how to establish a medical device quality system in a systematic, integrat ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Tell it to Your Doctor: Epilepsy
Harriet is 22. She developed myeloma at 15 and epilepsy at 17 and was treated for both conditions in several NHS facilities. In March 2006, she had a grand mal fit - a frightening major epileptic seizure that left her genuinely shaken. Eventually, after further seizures, she was diagnosed with juvenile myoclonic epilepsy.
After some pharmaceutical stabilisation, she attended Bath Spa University ...
Event at:
Wellcome Collection
in
London
-
United Kingdom
Type of Event:
Industry Events - Pharmaceutical - Medical
|
QbD Approach to Analytical Method Lifecycle: Design, Development, Validation, Transfer
This 120-minute webinar on using the QbD Approach to Analytical Method Lifecycle is designed to provide participants with a lifecycle approach to developing and validating analytical methods and comply with compendial requirements.
This webinar is designed to provide participants with a lifecycle approach to developing and validating analytical methods. By using a lifecycle approach, methods are ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
You have a Sterility Failure or Bioburden Excursion - Now What?
This Sterility or Bioburden test Webinar/training will discuss on various items that should be investigated to determine the root cause and the follow up to the investigation.
Why Should You Attend:
All sterile products require some level of sterility and bioburden testing during validation and then during routine production. What actions your company takes when this testing exhibits results ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Foreign Manufacturing Facilities – Avoiding Problems with FDA
This 90-minute webinar on compliant foreign manufacturing facilities will help you understand the problems that can occur with foreign manufacturers of pharmaceuticals. Recent inspections and enforcement actions by FDA have brought the topic into greater focus.
The FDA regulates foreign manufacturers of pharmaceuticals to be imported into the United States. Remote monitoring of quality assurance ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
FDA's Oversight of Mobile Medical Applications for Use on Smartphones and Similar Mobile De
This 90-minute webinar is designed to provide attendees with an overview of the U.S. Food and Drug Administration's oversight of certain medical and healthcare mobile medical applications ("apps") designed for use on smartphones and other mobile computing devices. You will learn to distinguish between those apps requiring FDA review and those not subject to regulatory oversight.
To ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Medical Device Risk Management Using ISO 14971
This webinar explains the application of Risk Management for medical devices using ISO 14971:2007. It explains the flow of information from the Risk Management Plan to the Risk Management Report, looking at important terms including Hazard, Harm, and Risk and explaining how to use each one. The program describes development of a Risk Evaluation form that implements the requirements of ISO 14971.
...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Water System Mythology: Common False Beliefs for Microbial Control and Monitoring
This water systems webinar training will discuss the myths surrounding microbial monitoring and control approaches and alert you to the pitfalls of believing these myths which could cause over-confidence in a system’s design for microbial control or the suitability of your microbial test methods.
Why Should You Attend:
Many water systems have been designed and are monitored using a set of rul ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
Project Management To Meet CGMP Requirements
This Project Management training for FDA Regulated Companies will show how you can meet key FDA and EU MDD regulatory requirements for the project you manage. It will focus on proven tools and techniques for successful development and implementation of project management planning.
The FDA expects companies to manage projects formally -- to include regulatory requirements, design and/or change c ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
How to Survive a DEA Audit
This 2-hr webinar will cover DEA record-keeping and security requirements that any DEA registrant must comply with when handling controlled substances. It covers elements of what occurs during an unannounced inspection and the auditing methods.
Why Should You Attend:
DEA regulations pertaining to the record-keeping and security of your handling of controlled substances are very stringent. Fines ...
Event at:
Online Event
in
Palo Alto
-
United States
Type of Event:
Industry Events - Pharmaceutical - Medical
|
27th International Conference of Alzheimer-s Disease International
The 27th International conference will be opportunity to bring together everyone with an interest in dementia - staff and volunteers of Alzheimer associations, families, people with dementia, clinicians, interested professionals and scientists - to share and learn from one another. ...
Event at:
ExCeL London
in
London
-
United Kingdom
Type of Event:
Industry Events - Pharmaceutical - Medical
|