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Courses

  • 441 Request Info

    Webinar on Combination Products-The FDA's New Codifications of the cGMP Requirements Applicable to Combination Products

    The FDA has ensured that clear FDA requirements were in place for drugs, devices, biological produces as well as Human Cells, Tissues and Cellular and Tissue-Based Products (HCT/Ps). However, there were no regulations in place to clarify and explain the application of cGMP requirements for combination products. The FDA is seeking to change that with the issuance of a guidance document that describes and explains the final rule on cGMP requirements for combination products. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/COMBINATION-PRODUCTS-501219/JAN-2016-ES-TRAININGREGISTRY
  • 442 Request Info

    Webinar on Preparation is the Best Medicine: Getting Ready for OSHA's New Strict, Expanded Enforcement against the Healthcare Industry

    The Occupational Safety and Health Administration has announced a new and stricter enforcement policy for the healthcare industry. The new federal enforcement policy, OSHA's recent new Inspection Guidance for Inpatient Healthcare Settings, which identifies five major hazard areas that OSHA inspectors will now examine as part of every visit & Inspection to a hospital, nursing home and residential care facility. So, is your facility ready for OSHA's close exam? Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/OSHA-COMPLIANCE-501200/JAN-2016-ES-TRAININGREGISTRY
  • 443 Request Info

    Webinar on The Basics of Professional Regulatory Law: Licensure and Certification, with an Emphasis on Health Professions

    Overview: Today's educated professionals function in a maze of different educational and training requirements, which vary from state to state and from profession to profession. Nowhere than in health care is this more evident where multidisciplinary health care practitioners work together towards a common goal for the patient. What is a profession? What areas of work require the unique professional education, training, and experience that becomes mandated by the state? What work requires professional judgment and skill so as to be regulated by the government through mandatory laws applicable to an individual person practicing his or her chosen profession? Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 support@mentorhealth.com Event Link: http://bit.ly/The-Basics-of-Professional-Regulatory-Law http://www.mentorhealth.com/
  • 444 Request Info

    Webinar on FDA Regulation of Medical Device Software

    Overview: The Food and Drug Administration (FDA) was not empowered by Congress to regulate medical devices until May 28, 1976 when the Medical Device Amendments were added to the Federal Food, Drug, and Cosmetic Act (FDCA). Why should you Attend: To gain a fundamental understanding of FDA regulation of medical device software. Areas Covered in the Session: Definition of medical device software FDA's medical device software regulatory scheme Software validation Level of concern Speaker Profile: Thomas E. Colonna earned a bachelor of science in microbiology from the University of Sciences in Philadelphia (formerly the Philadelphia College of Pharmacy and Science), a Ph.D. in molecular biology from the Johns Hopkins University. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/1MCN2jf
  • 445 Request Info

    Webinar on Setting the ideal cGMP HVAC Design Requirements for Pharmaceutical Sterile and Sterile Facilities

    Overview: It was observed that there are misunderstanding between design intent HVAC designer and User (who is working on the field) where each party is focusing on his area! Areas Covered in the Session: GMP Fundamentals of Pharmaceutical HVAC System This part will discuss the benefits of HVAC system in pharmaceutical industries as well as discussing the contamination sources that must be prevented where this section will give information about how bad HVAC can be risky on both process. Speaker Profile: Majdi is dedicated and results-driven Q&V expert with a highly successful background with Pharmaceutical companies in both project and operation fields to achieve the best possible performance through the creation and execution of successful. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/1Fenw4m
  • 446 Request Info

    Webinar on Development and Implementation of an External Auditing Program as part of a Pharmaceutical Manufacturing Quality System

    Overview: The presentation will explain the need and implementation of a pharmaceutical manufacturing external auditing program as part of an overall GMP compliant Quality System. Why should you Attend: The use of chemical and material suppliers, contract manufacturers and contract testing lab is integral in today’s pharmaceutical manufacture. With ever increasing diversity of WW suppliers and complexity in the regulatory and scientific realm of pharma manufacture. Speaker Profile: Joseph Habarta Ph.D. is founder and principal of J. Habarta Consulting that provides specialized consulting and assistance in the areas of international GMP and quality for the biotechnology and pharma industries. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/1OFoeuk
  • 447 Request Info

    Webinar on Extending Your Drug's Life

    Overview: This course will describe how a pharmaceutical company can prolong the life of a drug product. The high cost of time, money, and man-hours to develop a new pharmaceutical drug requires that the company hang onto the drug especially during the patent period. Why should you Attend: Healthy pharmaceutical companies take pride in adding years to a pharmaceutical product's life. People who are responsible for this result are often promoted because of the positive effect on the company's health. Speaker Profile: Bob Kunka Ph.D. is an accomplished and respected scientist who contributed to the development of 28 approved pharmaceutical products in eight therapeutic areas. His expertise on international product development teams produced submissions. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/1gLXQjC
  • 448 Request Info

    Webinar on 2011 FDA Guideline on Process Validation

    Overview: The FDA in 2011 instituted its latest interpretation. Many have not chosen to take it seriously or change their business model. Why should you attend: This is a topic very near and dear to those who are involved with qualification and validation. Of all the topics regarding compliance this subject area has to be the most re-invented. Who Will Benefit: Compliance Personnel QA Personnel validation Personnel Speaker Profile: Louis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of experience in Quality Assurance, Quality Control, Validation, consent decree remediation as well as cGMP Compliance in the Medical Device and Pharmaceutical industries. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/1WhE3Zn
  • 449 Request Info

    Webinar on Software Verification and Validation Planning and Documentation

    Overview: The verification and validation of medical software is coming under increased scrutiny by the U.S. FDA. This webinar will address the use of the FDA, GAMP, 21 CFR Part 11, "Electronic Records" / "Electronic Signatures", and other applicable industry software validation models. Why should you attend: Software has become pervasive in medical devices themselves, and in the controlling, running and monitoring of medical product processes, whether they be in the pharmaceutical, medical device, biologics or dietary supplements industries. Speaker Profile: John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. Contact Detail: NetZealous - Compliance4All, 161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA. Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/ Event Link : http://bit.ly/1KNlp7R
  • 450 Request Info

    Webinar on 21st Century Validation

    Overview: The 'why' and 'what' and the events / background that have impacted validation over the last 25 years will be presented. The importance of an organization's Quality System for validation will be put into perspective to help attendees identify potential gaps in their validation programs. The presentation will discuss the importance of 'focusing on critical aspects' and having meaningful, well-written User Requirements Specifications as key elements on establishing a streamlined and simplified validation program for capital projects.
  • 451 Request Info

    Webinar on Establishment of Quality Systems

    Overview: Quality Systems are a fundamental aspect of all pharmaceutical and medical device firms. They are an expectation and regulated requirement. Exactly what constitutes a quality system is different depending on the firm and the culture. Defining quality systems and then tracing them properly back to the FDA definitions is paramount for compliance and regulatory inspection preparedness.
  • 452 Request Info

    Webinar on Developing an Effective CAPA Program for GMP Operations

    Overview: Having an effective CAPA documentation and tracking system are crucial to pharmaceutical operations. This system will allow personnel to identifying the root cause, corrective action taken, and verification stages. This session will discuss important components to create an effective CAPA system, determine different levels of actions to be taken, and training needed to prevent reoccurrence.
  • 453 Request Info

    How to Conduct Medical Device Risk Analysis Effectively

    Why companies are prone to having past problems in new devices? One of the main reasons seems to be the ?weak cognition.? It is usually the result of short term memory, inattention to details, insufficient vigilance, or multitasking. This unsafe work propagates unknowingly because of not engaged or disengaged employees, insufficient understanding of customer needs, splitting design among several designers, and ineffective risk analysis. Another big reason is that ineffective device management procedures often touted as 'best practices', are like a bad virus with long incubation period and no early warning, resulting into sudden catastrophic malfunction of the device. Most companies still hold individuals responsible for mistakes instead of fixing the management process. Marketing has the advantage of helping prevent past mistakes and improve efficiency of the device design. They have records of customer complaints for years.
  • 454 Request Info

    Medical Terminology - Online Course

    Accredited self-paced online Medical Terminology class. This class combines an interactive study experience with the convenience of the Internet. Students can enroll at any time and complete the course at their pace. Begin learning Medical Terminology today! College credit is available for an additional fee.
  • 455 Request Info

    Anatomy & Physiology - Online Course

    Accredited self-paced online Anatomy & Physiology course. This course combines an interactive study experience with the convenience of the Internet. Students can enroll at any time and complete the course at their pace. Start learning A & P today! College credit available for an additional fee.
  • 456 Request Info

    Course Online Introduction to ECG (EKG)

    We offer a fully accredited, self-paced online Introduction to Electrocardiography (ECG) course. This course combines an interactive study experience with the convenience of the Internet. Master the principles of electrocardiography with our online Introduction to ECG course.