DUBLIN–(BUSINESS WIRE)–The “Technical Writing for Pharma, Biotech and Medical Devices” conference has been added to ResearchAndMarkets.com’s offering.
The quality and clarity of written technical documents are vital to the success of pharmaceutical companies. Such documents are used in regulatory submissions, to report the outcome of development work to clients, to record the results of investigations and to guide the direction of internal projects. In this course, participants will learn how to analyze and present technical data in a clear and concise manner. The use of visual tools such as graphs and flow charts will be covered, together with the design of effective tables. Statistical tools for data reduction and analysis will also be covered. The elements of effective standard operating procedures will also be explained. A large part of the course will be spent in a workshop setting, where attendees will produce technical content for comment and evaluation. The workshop can either be based on participants’ own data or model data provided by the trainer.
Attendees will be expected to bring a laptop computer. By the end of the course, attendees will be able to:
Learning Objectives:
Agenda:
Day 01(8:30 AM – 4:30 PM)
08:30 AM – 08:59 AM – Registration Process, Meet & Greet
9:00 AM -10:30 AM
10:30 AM -10:45 AM Break
10:45 AM -12:00 Noon
12:00 Noon -1:00 PM Lunch
1:00 PM -3:00 PM
3:00 PM – 3:15 PM Break
3:15 PM – 4:30 PM
Day 02 (8:30 AM – 4:30 PM)
08:30 AM – 08:59 AM – Registration Process, Meet & Greet
9:00 AM -10:30 AM
10:30 AM -10:45 AM Break
10:45 AM -12:00 Noon
12:00 Noon -1:00 PM Lunch
1:00 PM -3:00 PM Report-writing workshop
3:00 PM -3:15 PM Break
3:15 PM -4:15 PM Report-writing workshop (continued)
4:15 PM -4:30 PM Final questions, feedback and close
Speakers:
Mark Powell
Fellow
Royal Society of Chemistry
Dr Mark Powell is a Fellow of the Royal Society of Chemistry (RSC) with over thirty years’ experience as an analytical chemist. Mark was Honorary Treasurer of the RSC’s Analytical Division and led a working group on continuing professional development until July 2016, when his term of office ended. Between 2003 and 2013, he was the Analytical Development Manager, and later Scientific Manager, of a UK-based contract research organization which specialized in early-stage oral drug development. During this time, he was responsible for method validation, verification and transfer activities, as well as the qualification of laboratory instruments and computerized data systems. In 2013, he set up Mark Powell Scientific Limited, which provides training and consultancy services to pharmaceutical companies. Mark has since enjoyed working with companies of all sizes around the world on a variety of training and consultancy assignments, and has recently co-authored a White Paper on Pharmaceutical Data Integrity for the laboratory supply company VWR.
For more information about this conference visit https://www.researchandmarkets.com/r/rxsdkv
Contacts
ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
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