- OVERVIEW AND WHY SHOULD YOU ATTEND
- AREAS COVERED AND LEARNING OBJECTIVES
- WHO WILL BENEFIT
This webinar 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. Examples will include new formulations, indications, and additional patient populations. Healthy pharmaceutical companies take pride in adding years to a drug’s patent process life. People who are responsible for this result are often promoted because of the positive effect on the company’s health.
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. As employees stay with the company and get older, there is often a fear that the company will not continue to keep a person employed especially as he/she gets closer to pension age. They need to get associated with a drug’s name and longevity.Click to View the Pricing Plan
Pharmaceutical companies have numerous areas that are associated with most drugs. In the business side marketing looks to prepare advertising to prescribers and potential patients. Pharmaceutical manufacturing areas develop a new formulation and their colleagues make the new product for millions of patients. Scientists working with animals obtain basic safety information for a particular population that does not have data in the past. Clinical scientists develop safety, pharmacokinetic, and efficacy data in man to form the core of the data needed to get approved. Regulatory colleagues interact with regulatory agencies and team members to prepare important documents.
This webinar will describe how a pharmaceutical company can prolong the life of a drug product using:
- New formulations,
- Indications, and
- Additional patient populations
WHO WILL BENEFIT
- Project Managers
- Formulation Development Professionals
- Preclinical Development Professionals
- Clinical Development Professionals
- Regulatory Compliance Professionals
Robert L. 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 with successful clinical strategies, sound matrix management of individual study teams, and effective interactions with regulatory agencies leading to successful IND, aNDA, and NDA approvals. Bob's experience in drug development stems from 24 years in the pharmaceutical industry at GlaxoSmithKline (GSK), Chugai-Upjohn, and GD Searle.
Prior to this, he was Assistant Professor at the University of Pittsburgh School of Pharmacy where he taught graduate and undergraduate courses in pharmacokinetics. Bob earned his Ph.D. in Pharmacokinetics at the University of North Carolina (UNC) at Chapel Hill and Bachelor of Science in pharmacy at the University of Illinois at the Medical Center in Chicago. While at UNC, he was honored to be named the American Foundation for Pharmaceutical Education Charles J Lynn and Syndor Barksdale Penick Memorial Fellow. Bob has been consulting (The Kunka Group, Inc.) since 2008.View all trainings by this speaker
Form I-9 and E-Verify, Getting and Staying Compliant
Speaker: Cathleen M HamptonPrice: $199
Moving from an Operational Manager to a Strategic Leader
Speaker: Chris DeVanyTime: 01:00 PM EDT | 10:00 AM PDT
Location: New York
Logistics Channel Incoterms Standards
Speaker: Dr. Rossano V. GeraldTime: 01:00 PM EDT | 10:00 AM PDT
Location: New York
Thank you for the spreadsheet webinar. The webinar was informative and helpful. Although many of the concepts are known and understood by Industrial and Process Engineers, it is always helpful to have a straightforward review. The spreadsheet will be beneficial in being able to help identify areas of risk and areas that may require some attention.
Benchmark Electronics , ******** Engineer
This was a very informative session, it did help my company by raising awareness in areas we lack policies. The only thing I would suggest get added to the session is direct information relating to Accounting, ex. Taxation rules for record retention as they are some records which a company is required to keep indefinitely.
First MCO, ***** Manager
Overall I found the video conference well organized and very informative. The presenter, Ronald Adler, was certainly extremely knowledgeable and presented the subject matter in a well organized, direct and succinct manner. Afford the attendee the ability to track and record paid attendance/activity without a lot of tracking and follow up in order to gather the necessary information required to record the CPEs earned and paid for.
Dynamic Marketing Systems, VP Finance & Human Resources
As this was our first experience, we did not know what to expect. I believe the webinar was informative and to the point, and explained to us the purpose of the I-9, and how the company can be affected by an audit. It really motivated us to review our files and bring them up to date.
Young Transportation, ****Coach****
I have participated in several webinars hosted by Compliance Global on various H&S topics. They are always precise, technologically-oriented, and easy to use and partake in to further my knowledge of current Health and Safety regulations and topics.