Creative Writing, Drawing, Storytelling and Memoir.Creativity is a talent we are all born with. But it needs practice to stay vibrant and grow.Come to explore your creative potential and see some of the most beautiful places in the world.
Creative Writing, Drawing, Storytelling and Memoir.Creativity is a talent we are all born with. But it needs practice to stay vibrant and grow.Come to explore your creative potential and see some of the most beautiful places in the world.
Opal Events is proud to present our next exciting conference Medical Devices Summit 2010 which will highlight hot button issues in the medical devices industry.
The conference focus will encompass regulation and compliance, as well as global issues, topics which affect not only the pharmaceutical manufacturers, but transportation companies, pharmacies, and patients as well, among many other interested partys
With key products suffering patent expiration in coming years, the need for new approaches to accelerate development of new chemical entities to treat severely unmet medical needs is more urgent than ever.
Opal Events will strive to offer it's guests the most up to date and important information on regulatory issues, new technologies, and possible partnerships.
The CSP Yield Optimization Conference & Expo is the first event of its kind focusing specifically on CSP Balance of Plant Engineering and Plant Output, in more detail and technical depth than any previous conference.
An annual event hosted by Leatherhead Food Research in the United States, providing an informal forum for US-based delegates to meet, stay informed and discuss topical food regulatory issues of EU and international interest.
The Creativity Workshop focuses on developing creativity skills in people from all disciplines: education, business, the arts, sciences, and social services. Come learn with us in an inspiring and nurturing atmosphere.
The Creativity Workshop focuses on developing creativity skills in people from all disciplines: education, business, the arts, sciences, and social services. Come learn with us in an inspiring and nurturing atmosphere.
This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel.
The session will review the guideline to cover the key areas of compliance including: The role of the "Qualified Person", Packaging, labeling, reconciliations that should take place for each product and each production stage.
This interactive one-day course provides a thorough understanding of what makes water systems have microbial problems with proven solutions for microbial control, arguments for the micro lab.
This Design validation 4 hour session will discuss how to write validation protocol and determine acceptance criteria. It will also explain the systematic approach to validate analytical procedures.
It is critical that a robust transfer program be put into place in order to head off issues. Unearthing issues at the drug development stage, rather than during routine manufacture, will improve the overall success of the project.
This contamination control webinar will discuss how personnel practices, transferring items into cleanrooms, facility design, construction, and sporicidal chemistries are critical .
This IFRS (International Financial Reporting Standards) webinar will discuss how to assign a fair value to financial instruments and how to comply with the changing rule for accounting for investment on financial statements.
Learn the scientific standards of drug development process, the regulations to follow in Phase I and how to manage each phase of drug development process.
This environmental monitoring training will review the best practices for setting environmental monitoring alert and action levels for viable and non-viable data including product bioburden.
This clinical research ethics training will impart an understanding to regulatory compliance and clinical study personnel on the importance of ethics in clinical research .
This course reviews the investigator TMF required and additional content for a clinical trial - the activities of set-up, maintenance, and quality control and assurance will be discussed, as well as common deficiencies and challenges.
Learn how to successfully pass a clinical trial audit, how to prepare for it, where and how to identify the non compliance. Know FDA inspection strategy to identify areas of common deficiency.
This Integrated Risk Management Approach training in ISO 14971 will discuss how to incorporate risk management as per ISO 14971 in all phases of medical device development.
This presentation will review the QSR requirements for document change control, and provide a streamlined process - Many companies can spend MUCH LESS preparing MANY FEWER documents, and still be in compliance with the regulations;
This Medical device inspection webinar training will teach you A to Z of inspection starting with how to prepare to what to do during inspection, close-out interview, FDA
This Ethylene Oxide Sterilization Residuals regulation based webinar will provide a practical approach to fulfill requirements of the new ISO EO residual limits revised regulation.
This Medical device complaints handling webinar will discuss the best practices of complaint handling and how to include it in your CAPA program and how to apply risk management to the complaint handling system.
A detailed understanding of process validation for medical devices approach employing IQ, OQ, and PQ. Information to include in the protocols and reports, Statistical Process Control, Design of Experiments, usage of attribute.
This Pregnancy Discrimination claims related training will provide essential strategies for ensuring that those rights are observed while at the same time allowing for the smooth operation of your organization.
This webinar provides an update of federal and state UI issues, assesses the risks and costs associated with UI taxes and benefits, and discusses effective UI tax management and cost control techniques.
This health care reforms webinar will discuss the various categories of employer under health Care reform, impact of the reform and the steps to be ready for upcoming implementation dates.
These are just a few of the nightmares that keep HR professionals awake at night. If these are the kinds of employee problems that are haunting you, we promise this webinar will help you get a better night
Learn in details how to accurately and completely process garnishment orders through the payroll department in compliance with federal and state requirements and regulations.
This webinar will describe the distinctions that must always exist between contractors and employees based on standards used by the federal Department of Labor.
Learn steps to create a fool proof retention process and strategies for effective employee involvement and the low cost ways to motivate and energize employees.
Auditing and Administrating Human Resource Policie
This HR compliance virtual event will discuss about HR risk assessment, Recordkeeping, Retention and Destruction, Selecting and Administering Employment Policies, Legal Interviewing and Hiring Practices.
This webinar delves into what to (and not to) do when you receive communications from the IRS and also what to do when doing business with other federal, state and local regulatory agencies and lawmaking bodies.
In this CSV seminar learn how to reduce validation project time, efficient documentation strategies, enhance system productivity and increase compliance with the New 21 CFR Part 11 regulations.
Understand 10 step Risk based approach to validation, explore methods to decrease resource requirements and make documentation more manageable and understandable.
This Food Safety training will teach you about how to use problem solving method steps and tools to eliminate the reoccurrence of process & product non-conformities .
In this HACCP webinar learn the required elements of conducting and documenting CCPs and process parameters and the five sources of HACCP validation as per FSIS guidelines.
Learn how to differentiate and draw boundaries for GMP and GLP practices if done in same laboratory and how to transition a procedure in development to one used routinely.
This highly interactive course will include detailed discussions of current regulatory expectations and is therefore suitable for individuals new to the pharmaceutical industry and also serves as a refresher course for others.
When you get your 510(k) how to market your 510(k) , what communication strategy to adopt, what to do when FDA disagrees with your promotional positioning.
In this Audit training learn how to make audit checklist an effective tool, by improving it through restructuring to drop the canned clause-based questions and identify the expected evidence.
Attend this webinar to understand the process of a letter of credit and how to comply with letter of credit requirements to help reduce or prevent costly discrepancies.
In this Foreign Corrupt Practices Act (FCPA) webinar training understand the prohibited and exempted actions as per FCAP act, how to find the non compliance issues and how to implement FCPA compliance policies.
Webinar On Obtaining and Maintaining EU Compliance
This CE marking training will discuss the recent changes to MDD (Medical Device Directive), how to identify non compliance areas, contents of the technical file and essential requirements document.
2nd Annual HCC Best Practices for Proactive Medica
This conference will build on the success of the 2010 conference while providing practical, timely updates to help you continue to evolve your medical management practices with sound HCC coding
2nd Annual Medical Management in Medicare Advantag
With over 200 attendees at our launch event, our Collaborative Care Summit has established itself as one of the premier Medical Management conferences.
In today's turbulent financial environment, the need has never been greater for officers and trustees of pension funds to stay abreast of the constant changes and anticipated trends.
Opal Financial Group's Clean and Green Investment Forum will bring together experts from throughout the country to discuss the most important topics in cleantech and greentech.
BiOS is the world's largest and most prestigious international biomedical optics and imaging conference, encompassing clinical, translational, and fundamental R&D.
Share your research and development activities with colleagues, sponsors, customers, technologists, engineers, scientists, and clients in the growing industry of Micro- and Nanofabrication of MEMS and MOEMS.
OPTO 2012 addresses the latest developments and advances in a broad range of optoelectronic technologies and their integration for a variety of applications.
ION ITM 2011 features more than 150 technical papers, large international participation, and a diverse array of topics on positioning, navigation and timing.