World Conference Calendar

31707 Conferences

Physical and Life Sciencesrss


Pre-Demolition Engineering Survey - Webinar By ComplianceOnline

Pre-Demolition Engineering Survey - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-27-2012 Last Day: 01-27-2012
This webinar will help you understand OSHA’s requirement for a pre-demolition engineering survey, including what documents to have in place, for renovation and complete demolition of buildings/structures. Why Should You Attend: Due to the significant number of fatalities, injuries, fires, spills/releases, and “near misses” in construction/demolition activities OSHA requires an engineering survey to be made by a “competent person”. That person may be a professional engineer (PE), certified safety professional with demolition experience, or a demolition contractor employee with adequate experience and communication/writing skills. The survey may be brief for small structures or extensive for large facilities. Due to unauthorized…
3rd Annual Health Outcomes and Pharmacoeconomics Research Conference

3rd Annual Health Outcomes and Pharmacoeconomics Research Conference

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-30-2012 Last Day: 01-31-2012
Continuing in its Health Outcomes series, marcus evans invites you attend the two-day, industry focused event, specific to those within Outcomes Research, Global Health Outcomes and Health Economics. Hear from industry leaders within Bio/Pharmaceutical and Medical Device companies such as: Novartis Pharmaceuticals, Inc., Endo Pharmaceuticals, BD, Abbott, Takeda Pharmaceuticals, EMD Serono, Inc., Baxter Healthcare and many more! Attending this conference will allow attendees to walk away with key best practices for conducting successful outcomes research and applying pharmacoeconomics deeper into the brand management, product development and commercialization strategies of the Pharmaceutical industry. Attendees will also be provided with useful and…
Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems

Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-02-2012 Last Day: 02-02-2012
Why Should You Attend: This interactive one-day course provides a thorough understanding of what makes water systems have microbial problems with proven solutions for microbial control. It also details how to validate that control by determining the operations and processes that logically must be evaluated in pharmaceutical water and steam systems during the validation exercise in a manner that will please FDA. Finally, and perhaps most importantly, attendees will learn how to institute simple sampling, monitoring and microbial control levels that will dramatically reduce microbial excursions and facilitate having successful and accurate root cause investigation outcomes. In short, if your…
3-hr Virtual Seminar - Safety; How, Do I Get Started

3-hr Virtual Seminar - Safety; How, Do I Get Started

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-03-2012 Last Day: 02-03-2012
This OSHA compliance training will help you understand the importance of getting started as a safety professional and where to start. You will also learn the importance of getting management buy-in. The beginnings of your career in Safety can be intimidating - wondering where to start, You have been asked if the employees have been trained to operate a piece of equipment and you answer with that confused look, your insurance company wants the latest OSHA 300 log and you have no idea, the company president wants the safety committee meeting minutes, you don’t have one in place – this…
3-hr Virtual Seminar: Medical Device Regulations and Law in the US, EU and Canada

3-hr Virtual Seminar: Medical Device Regulations and Law in the US, EU and Canada

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-07-2012 Last Day: 02-07-2012
This 3-hr training will discuss medical device regulations and law in the US, Europe and Canada. It is designed to help the audience with their global compliance and regulatory intelligence, which is necessary to streamline the regulatory process in an organization to achieve sustainability and to remain sustainable and competitive in global markets. This seminar is a “How To Guide” intended to streamline the decision-making process in a systematic manner. Why You Should Attend: The global regulation of medical devices is rapidly evolving, integrating the regulatory systems of the most advanced medical device regulations. To be able to achieve sustainability…
Medical Device Process Validation - Statistical Considerations

Medical Device Process Validation - Statistical Considerations

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-08-2012 Last Day: 02-08-2012
This Process Validation training will look at the underlying statistical concepts to perform an effective process validation. The webinar examine elements of the FDA regulations for process validation (21 CFR §820.75) as well as the corresponding requirements in ISO 13485. The FDA’s Quality system regulation requires device manufacturers to validate processes when they don’t fully verify the resulting output. Based on Warning Letters, the FDA expects manufacturers to validate processes when the output check uses sampling instead of 100% inspection. The presentation looks at these aspects of process validation using the unifying approach of a statistical model. Rather than a…
Setting up an effective Internal Audit Program - Webinar By ComplianceOnline

Setting up an effective Internal Audit Program - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-08-2012 Last Day: 02-08-2012
This 90-minute Internal Audit webinar will cover the three foundational elements that support an effective Internal Audit program - establishing Internal Audit Program objectives, developing audit plans, and writing effective non-compliances. Why Should You Attend: Internal auditing drives continual improvement and reminds everyone that Quality comes first! Auditing is an assessment tool that provides a reliable performance indicator of your organization’s system and processes. In other words, an internal audit is an audit of an entity's internal control systems and procedures and how the system and procedures are implemented. Companies that establish internal audits as part of their culture to…
Life Cycle Validation of GMP Potency Bioassays - Webinar By ComplianceOnline

Life Cycle Validation of GMP Potency Bioassays - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-09-2012 Last Day: 02-09-2012
This 90-minute webinar will provide guidelines for bioassay validation and regulatory documentation, the steps for technology transfer and commercial validation show how to implement the new USP chapters 1032, 1033 and 1034. Why Should You Attend: Potency bioassays are an integral part of release testing and stability studies for biotechnological products. There is a lack of clarity of how much work is required at each development phase to maintain scientific rigor and meet regulatory expectations. This webinar provides a logical plan to progress the potency bioassay from a tool to assist in pre-clinical process evaluation throughout final commercial implementation. The…
Managing OSHA Inspections and Accident Investigations

Managing OSHA Inspections and Accident Investigations

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-10-2012 Last Day: 02-10-2012
This OSHA Inspection and Accident Investigation training will provide practical tips for safety professionals and managers on what the OSHA inspectors will look for, how to respond to a letter of complaint, how employees and unions figure into the inspection equation, and what you must do to expedite the inspection and help resolve issues before they become major problems. Why Should You Attend: Perhaps of all of the interactions that occur with regulatory agencies, the unannounced OSHA inspection is the most stressful, and least understood by business owners. The key to managing a surprise OSHA Inspection or a letter of…
Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations

Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-13-2012 Last Day: 02-13-2012
This contamination control webinar will discuss how personnel practices, transferring items into cleanrooms, facility design, construction, and sporicidal chemistries are critical and how it can be addressed in developing a successful contamination control program. Areas Covered in the Seminar: * Developing effective ways to address spore excursions. * Troubleshooting real world experiences. * Developing preventative action plans. * Learn ways to improve facility design and maintenance. * The most effective sporicidal chemistries will be discussed in detail. * Cleaning and Disinfection Methods will be addressed. * Warning Letters and 483’s from FDA will be discussed and addressed. Who Will Benefit:…
Environmental Monitoring and Contamination Control Plan

Environmental Monitoring and Contamination Control Plan

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-15-2012 Last Day: 02-15-2012
This 90-minute cleanroom contamination control training will review the common mistakes that people make in cleanrooms that lead to contamination, show how to develop a successful contamination control program and discuss ways to improve your facility's design and maintenance. Why Should You Attend: This 90-minute presentation will review the basics of personnel practices and discuss cleaning and disinfection. The most common source of contamination in the cleanroom are people and as such it is important to cover common mistakes in behavior and gowning. The speaker will address facility design and conditions as well since these are also a contributor to…
CRO or ARO: How to Hire and Manage One

CRO or ARO: How to Hire and Manage One

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-15-2012 Last Day: 02-15-2012
This training on hiring and managing CROs or AROs will show how you can ensure that you choose the right CRO/ARO based on the phase of the trial, the therapeutic area and the countries that the trials will be conducted. Why Should You Attend: A critical component in successful Clinical Research Trials is ensuring that you choose the right CRO/AOR based on the phase of the trial, the therapeutic area and the countries that the trials will be conducted. It is then important that the scope of the work be clearly defined to ensure that budget and timelines are respected…
3-hr Virtual Seminar - OSHA Asbestos and Mold Awareness: All-in-One Session

3-hr Virtual Seminar - OSHA Asbestos and Mold Awareness: All-in-One Session

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-17-2012 Last Day: 02-17-2012
This 3-hr virtual seminar - OSHA Asbestos and Mold Awareness - will cover OSHA's regulations on Asbestos and specific guidelines and general regulations on Mold. Why Should You Attend: Asbestos is one of the most highly regulated substances, and for good reasons as it’s a potent carcinogen with no known safe exposure. Of all of the toxic and hazardous substances it could have regulated, OSHA chose to regulate Asbestos first. Mold, on the other hand, is an even more ubiquitous contaminant in buildings, yet OSHA has not even attempted any regulations specific to it. Instead, they have a set of…
International Conference on Product Development and Renewable Energy Resources – ICPDRE 2012

International Conference on Product Development and Renewable Energy Resources – ICPDRE 2012

Location: , India
Category: Physical and Life Sciences
Start Date: 02-18-2012 Last Day: 02-19-2012
ICPDRE 2012 will be held during February 18-19, 2012 in Coimbatore, India. ICPDRE 2012, is to bring together innovative academics and industrial experts in the field of Product Development and Renewable Energy Resources to a common forum. The primary goal of the conference is to promote research and developmental activities in Product Development and Renewable Energy Resources. Another goal is to promote scientific information interchange between researchers, developers, engineers, students, and practitioners working in India and abroad. The conference will be held every year to make it an ideal platform for people to share views and experiences in Product Development…
Cell Line Development & Engineering Asia

Cell Line Development & Engineering Asia

Location: , China
Category: Physical and Life Sciences
Start Date: 02-20-2012 Last Day: 02-23-2012
CELL LINE DEVELOPMENT & ENGINEERING ASIA brings together experts and top scientists from biopharmas, biotechs, CMOs and research institutes as well as leading technology providers from Asia and globally. The region’s 1st and ONLY focused Cell Line Development and Engineering Asia provides a forum where industry experts share lessons learned through case studies, strategic discussion groups and interactive roundtables to collectively collaborate and provide solutions to your most pressing challenges. Bring back new ideas to do better business. Key themes and issues include: 1.Examining the Business and Regulatory Landscape 2.Cell Line Development Approaches for Biosimilars 3.Addressing Timeline Bottlenecks in Development…
Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction

Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-20-2012 Last Day: 02-20-2012
This 90-minute webinar on Advanced Methods of Root Causes Analysis, for medical device companies, will cover principles and methods of Root Cause Analysis (RCA) and review proven techniques for ISO 14971 Risk Reduction based on RCA. Why Should You Attend: Root Cause Analysis (RCA) is the most important tool in device recall investigations and for preventing the adverse events. Unfortunately there is substantial misunderstanding of the limitations of the tool and how to use it correctly. The result is often wrong judgments, wrong design changes, and wasted efforts. Doing it right will reduce costs. Using advanced methods will make a…
Implementation of Pharmacogenomics into the Routine Clinical Laboratory

Implementation of Pharmacogenomics into the Routine Clinical Laboratory

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-22-2012 Last Day: 02-22-2012
This 90-minute webinar will cover the basic principles of pharmacogenomics and pharmacogenetics and will discuss in detail the steps behind implementing a clinical pharmacotenomic testing service. Why Should You Attend: The FDA's Center for Drug Education and Research has relabeled many drugs recommending pharmacogenomic testing. In other cases, the FDA has issued "black box" warnings cautioning doctors that there are genetic variances that effect safety profile for drugs such as codeine and clopidogrel. These FDA mandates have driven the adoption of pharmacogenomic testing into clinical practice to date. Pharmacogenomic laboratory tests are available for these drugs.Adverse events caused by these…
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems

The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-22-2012 Last Day: 02-23-2012
All pharmaceutical, biologics, and medical device facilities are likely to have high purity water systems. In spite of this purity, microorganisms can flourish within these systems and lead to undesirable contamination of facility processes and their products. Of all the individuals at the facility who should understand the microorganisms in water systems and how best to monitor and control and them, it should be the site’s microbiologists. Sadly, this is often not the case due to the lack of familiarity with biofilm and its impact on water system sampling, testing, sanitization, and routine maintenance. This course is designed to provide…
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems

The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-22-2012 Last Day: 02-23-2012
All pharmaceutical, biologics, and medical device facilities are likely to have high purity water systems. In spite of this purity, microorganisms can flourish within these systems and lead to undesirable contamination of facility processes and their products. Of all the individuals at the facility who should understand the microorganisms in water systems and how best to monitor and control and them, it should be the site’s microbiologists. Sadly, this is often not the case due to the lack of familiarity with biofilm and its impact on water system sampling, testing, sanitization, and routine maintenance. This course is designed to provide…
Accelerating Bioassay Transfer in a GMP Environment - Webinar By ComplianceOnline

Accelerating Bioassay Transfer in a GMP Environment - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 02-23-2012 Last Day: 02-23-2012
This Bioassays webinar will systematically outline the steps needed to successfully transfer validated biological assays between GMP/GLP labs and also acquire non-validated assays for GMP/GLP development. Why Should You Attend: 50% of the drugs presently in discovery are biopharmaceuticals - these numbers lead to an "outsource or perish" philosophy for GMP/GLP development, validation and sample analysis. Unlike synthetic drugs requiring only straightforward analytical testing biopharmaceuticals require more elaborate assays to attain regulatory compliance. The industry has a significant underestimation of the discipline; skills and planning required to successfully transferring these assays. Naiveté in this area causes loss of precious time…

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