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  • 1041 Request Info

    Webinar on SOPs for Clinical Trials: Regulatory Requirements

    Since the year 2000 there has been an increasing trend of registered clinical studies from approximately 4,000 in 2000 to 160,000 in 2014. In 2014 Forbes Magazine reported that the FDA had approved 44 drugs the highest in 18 years. As innovation and new technological approaches are applied to the discovery of novel molecules, the number of studies will continue to increase to meet the areas of unmet medical needs and especially rare diseases. Clinical currently list 193,510 studies in 50 states and in 190 countries.
  • 1042 Request Info

    Webinar on Identity Theft and Health Care Fraud

    Overview: Healthcare fraud is a growing scourge on our already weakened healthcare industry. Healthcare fraud and abuse costs consumers $85 billion per year, and this astronomical figure does not even include disability, workers' compensation, property and casualty, and life insurance. As the costs of healthcare expenditures are expected to exceed $1.8 trillion, healthcare fraud accounts for: Between 3% and 10% of the total healthcare dollars spent 20% to 30% of the total dollars spent as a result of abusive billing practices A $400 per household increase in premiums every year Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 Event Link:
  • 1043 Request Info

    Webinar on How to Handle HIPAA Security Incidents, Breaches, Complaints, and Investigations

    Overview: This webinar will cover everything that you need to know about how to handle HIPAA security incidents, breaches, and complaints and the Department of Health and Human Resources Investigations thereof. Not all security incidents are breaches, but all breaches of confidentiality are within the broad ambit of security incidents. Privacy rule violations, such as failing to give a patient a copy of his or her medical records, may also constitute a breach as the $4.2 million fine assessed against Cignet Healthcare of Prince George's County, Maryland, dramatically proved. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 Event Link:
  • 1044 Request Info

    Webinar on Update to OSHA Hazard Communication Law

    Overview: This webinar will provide employers and employees with the new requirements for the Hazard Communication Standard, as well as the changes in the regulations, the way chemicals are classified, and what will be new for training and Safety Data Sheets. Why should you attend: Employers who use, manufacture, supply or import hazardous chemicals need to be aware of the new regulations and how they affect their employees and their businesses. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 Event Link:
  • 1045 Request Info

    Webinar on The Federal False Claims Act and the Anti-Kickback Statute: Is Your Organization at Risk

    Overview: The session will provide an overview of the Federal Civil False Claims Act (FCA) and how it works. It will also provide an assessment of enforcement activities, showing how participants may be at risk. In addition, the session will review recent cases and show how they potentially impact participants. We will start with a review of the Federal False Claims Act and discuss how it works and how it is being used to fight health care fraud. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 Event Link:
  • 1046 Request Info

    Webinar on Medical Coding for Dental Sleep Apnea Treatment

    Overview: This webinar will provide the information that dental practices need to be able to truly help their patients afford this life saving treatment. All areas of helping dental practices implement this profit boosting system will be discussed. Dental practices have experienced a paradigm shift over the last decade due to the research into the systemic link. Dentistry has now become the field of dental medicine. With regard to that shift, one area of significant change is with obstructive sleep apnea. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 Event Link:
  • 1047 Request Info

    Global Review of Sunscreen Science, Products and Regulation

    To formulate a successful sunscreen product for topical application requires a multidisciplinary approach. Factors need to be taken into consideration include the current market trends & demands, regulatory framework & compliance requirements, scientific learning on skin structure and function, UV-interacting chemistry & science, and appropriate delivery systems for optimal effectiveness and safety. This course will provide an overview of sunscreen regulations and technologies that enable the participants to design proper strategies for successful product development and marketing. In addition, small group discussion / workshops on real-life case studies will be conducted throughout the course to familiarize the participants with the complex regulatory framework and product labeling & advertising guidelines.
  • 1048 Request Info

    Webinar on Recent HIPAA changes in 2016: Are you in Compliance?

    This live training session will address the major changes under the Omnibus Rule and any other applicable updates for 2016. There are an enormous amount of issues and risks for covered entities and business associates under Omnibus, first and foremost being the Feds have an increased budget and enforcement abilities via utilizing outsourced auditing.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 1049 Request Info

    Webinar on Civil Rights Case Law Guideline for HR Professionals

    It is almost impossible for managers and HR professionals to stay current in the ever evolving civil rights case law due to their busy workload. As a result, discrimination and harassment may go unrecognized and allowed to continue creating a hostile work environment for employees resulting in absenteeism, turnover, loss of productivity and physical and emotional health consequences to the target and witnesses of the abuse.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 1050 Request Info

    Online Webinar on Blue Print for Implementing Pharmaceutical and Medical Device Quality Management System under one Umbrella

    In this webinar, the presenter with 1st hand proficiency in setting up and speaking the quality language of medical device and the pharma world will provide unique tips for those companies that are making the transition from medical device to pharmaceuticals and vice versa.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 1051 Request Info

    Online Webinar on USP [467] Residual Solvents: Overview of General Principles and New Additions

    This training will provide an overview of General Chapter USP <467> requirements for testing of residual solvents and limits, along with providing updates on the new content added to provide greater flexibility in testing compliance.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 1052 Request Info

    Online Webinar on Using an IQ / OQ / PQ Approach to Validating Medical Device Software

    This medical device software validation training will show how you can validate software using IQ / OQ / PQ methodologies, typically employed for medical device process validation. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 1053 Request Info

    Online Webinar on Clinical Evaluation and Risk Management

    Medical devices sold in the European Union fall under the Medical Device Directive (MDD). The webinar includes a discussion of clinical evaluation, including the recommendations from MEDDEV 2.7-1 Clinical Evaluation: A Guide for Manufacturers and Notified Bodies. The webinar also covers MEDDEV 2.12-2 Guidelines on Post Market Clinical Follow-Up. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 1054 Request Info

    Webinar on HVAC and GMP Environmental Control - for Pharmaceutical Cleanrooms

    This webinar details and explains the various US and international regulatory requirements for various cleanroom classifications. Environmental control of pharmaceutical cleanroom is essential to the manufacture of a quality product. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 Event link
  • 1055 Request Info

    Conference about Introduction to FDA Regulation of Combination Products

    Overview: A combination product is a product composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device, and a biological product. Under 21 CFR 3.2 (e), a combination product is defined to include: A product comprised of two or more regulated components (i.e., drug/device, biologic/device, drug/biologic, or drug/device/biologic) that are physically, chemically, or otherwise combined or mixed and produced as a single entity.
  • 1056 Request Info

    Conference about Managing Non-Conformance and Corrective Actions

    Overview: Root Cause is an essential component for addressing non-conformance. It uses a specific set of steps, with associated tools, to find the primary cause of the problem, so that you can: Determine what happened. Determine why it happened. Figure out what to do to reduce the likelihood that it will happen again. RCA assumes that systems and events are interrelated. An action in one area triggers an action in another, and another, and so on. By tracing back these actions, you can discover where the problem started and how it grew into the symptom you're now facing.
  • 1057 Request Info

    Conference about Proven Cleaning and Sanitation Techniques for Food Processors

    Overview: Cleaning and sanitation programme are essential to control the hazards of microbiological and physical contamination of foods in the foodservice and food manufacturing facilities. To ensure that a facility and equipment are clean, sanitised and suitable for their intended use, management of the food business must draw up and operate a written sanitation programme and suitable cleaning procedure for all equipment surfaces and structures within the facility. This webinar will offer the participants unambiguous cleaning and sanitation templates for High care and Low risk areas.
  • 1058 Request Info

    Conference about Safe Drinking Water-Another Oxymoron

    Overview: This webinar will look at the historical use of indicator organisms to define the safety of drinking water and will examine the limitations of this approach for evaluating water potability. Waterborne outbreaks will be reviewed in the context of identifying the wide etiological scope and the inability of traditional indicators to mitigate these risks. Alternate considerations for assessing potability will also be discussed.
  • 1059 Request Info

    Conference about Sanitizers for the Food Industry

    Overview: Effective sanitation in the food industry involves the maintenance of clean conditions in the entire food operation. This status is attained through the destruction of residual microorganisms after cleaning of production, storage and service areas of food establishments. As the food processing and foodservice industries have grown, methods of food production, processing, distribution, and preparation have changed. Increased processing and food preparation have included more prepackaged food as partially or fully prepared bulk or pre-portioned servings and centralized food production.
  • 1060 Request Info

    Conference about Validation Master Planning and Regulatory Expectations

    Overview: Our Speaker will explain the expectations of regulatory authorities both domestic and international. You should attend if you are not familiar with the activity or would like to understand the expectations both foreign and domestic. This presentation will cover the importance of master planning. The FDA and other regulatory bodies expect these to be among the Quality System documentation. How best should it be implemented and maintained? What are the types and how many should there be?