Regulatory Affairs Academy
-Building your Regulatory Affairs and Life Science competence
Register to Regulatory Affairs Academy
What is Regulatory Affairs Academy?
The Regulatory Affairs Academy by Läkemedelsakademin (the Swedish Academy of Pharmaceutical Sciences) gives you
- knowledge of the regulatory requirements for the different phases of drug development, before and after product approval*, on a global level, emphasising on Europe
- skills to plan, project manage and carry out the regulatory work to support optimized drug development, product safety and availability on the market and ensure that the companies meet the regulatory requirements set by authorities
- competence to interpret and analyse the regulations to be able to both operate and advise during the different phases of drug development before and after product approval*.
*Medicines Agency authorisation to market a medicinal product in a specific country
Regulatory Affairs Academy consists of 11 separate courses, altogether covering the regulatory role and requirements in the different phases of drug development before and after product
The content is well-structured and provides a comprehensive picture of regulatory affairs, from early drug development to marketing. The lecturers are very committed and happy to share their expertise and experiences from the industry.
I highly recommend the training and think it is valuable for anyone interested in Regulatory Affairs, regardless of whether you are new or have previous experience.
For whom?
The Academy is meant for you who aim to work within regulatory affairs for the pharmaceutical industry. You may already have started your regulatory affairs career and need to further build and update your knowledge and skills, or perhaps you work within another part off the life science sector right now, but have your sights set on a position within the regulatory affairs area.
Your recommended prerequisites to be able to fully benefit from the education and to be an attractive future employee in the life science industry after completing the education is: a degree in for example pharmacy, biomedicine, medicine, molecular biology or chemistry, or professional experience where equivalent knowledge has been acquired.
What is included?
11 stand-alone courses developed by Läkemedelsakademin together with industry experts, in a package that offers a 25% discount compared to buying the courses individually
A personal Diploma from Läkemedelsakademin showing your education in Regulatory Affairs
A personal membership in Apotekarsocieteten (the Swedish Pharmaceutical Society) during the time of your education
25% discount on additional courses and events offered by Läkemedelsakademin within the Regulatory Affairs area during the time of your education
Program execution and format
The training program enables a combination with other studies or work.
We want your educational journey to be agile. Therefore, all included courses can be completed online from your preferred location
– whether that is from home or from your workplace, in consultation with your employer.
The courses are carried out as online live seminars with lecturers, pre-recorded seminars of lecturers or e-learnings.
For some of the live seminars, there may be opportunities to participate live on site in Stockholm if you wish and if seats are available.
Our initiatiors, sponsors and partners
The life science industry in Sweden is a great place to learn the regulatory work. Sweden has and has had large companies functioning as nurseries for many regulatory professionals. In addition, the Medical Products Agency takes on a lot of responsibility in the EU work and persons from their staff find their way out to pharma companies and vice versa. Sweden is also a small country where many people know each other and can share experiences on a network basis, e.g. through Apotekarsocieteten. Läkemedelsakademin also plays an important role, with courses that continuously develop people throughout working life. Skills development is needed, not only for individuals but also for the Swedish pharma industry. This is to maintain a strong position when the company structure is shifting towards a larger amount of smaller companies where it can be more difficult to build a broad expertise.
Read more from the other initiators, sponsors and partners behind the program
Investment
- Participation fee excl. VAT (for companies): 63 900 SEK
- Participation fee incl. VAT (for individuals): 79 875 SEK
Partial payment is possible. Contact us for more information.
Läkemedelsakademin reserves the right to postpone or cancel included courses at any unforeseen event. Should this happen, participants in the Regulatory Affairs Academy program receive a voucher for the course’s regular price, to use for any course in Läkemedelsakademin total current course offering within 2 years.
RAA gives me access to information in detail in all the relevant areas. This is invaluable to me. It is so fantastic to get the access to Sweden’s top experts in the regulatory field and to the experts at one of Sweden’s most important authorities: the Medical Products Agency. What I learn now will help me onwards in my contact with the authorities. It will help me asking the right questions and talking to the authorities efficiently.
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Nödvändiga
Dessa kakor går inte att välja bort. De behövs för att hemsidan över huvud taget ska fungera. -
Statistik
För att vi ska kunna förbättra hemsidans funktionalitet och uppbyggnad, baserat på hur hemsidan används. -
Upplevelse
För att vår hemsida ska prestera så bra som möjligt under ditt besök. Om du nekar de här kakorna kommer viss funktionalitet att försvinna från hemsidan. -
Marknadsföring
Genom att dela med dig av dina intressen och ditt beteende när du surfar ökar du chansen att få se personligt anpassat innehåll och erbjudanden.