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Category: Regulatory news

Home / Regulatory news

Regulatory online workshop on medical devices: COMPLIANCE CHECK OF MEDICAL DEVICES PRIOR TO MAKING THEM AVAILABLE IN THE MARKET

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On 15/02/202215/02/2022By rapharmIn Current educations and trainings, Regulatory news, Uncategorized

6th & 7th April 2022 Microsoft Teams (Slovenian language) Regulatory online workshop on medical devices: COMPLIANCE CHECK OF MEDICAL DEVICES PRIOR...

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Regulatory 3-day online workshop on medical devices: GOOD PRACTICES TO MEET THE REQUIREMENTS OF NEW LEGISLATION IN THE FIELD OF DISTRIBUTION AND IMPORT OF MEDICAL DEVICES

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On 15/02/202216/02/2022By rapharmIn Current educations and trainings, Regulatory news

22nd, 23rd & 24th March 2022 Microsoft Teams (Slovenian language) Regulatory 3-day online workshop on medical devices: GOOD PRACTICES TO MEET...

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We welcome new colleagues to our team!

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On 01/04/202121/06/2021By rapharmIn Regulatory news, Uncategorized

Due to the many opportunities and challenges that lie ahead, we would like to welcome new colleagues to our team!...

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Regulatory workshop on medical devices: COMPLIANCE CHECK OF MEDICAL DEVICES PRIOR TO MAKING THEM AVAILABLE IN THE MARKET

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On 04/12/201925/10/2021By rapharmIn Current educations and trainings, Regulatory news, Uncategorized

Third term: 26th March 2020 – CANCELLED (COVID-19) raPHARM premises, 30 Miklošičeva Street, Ljubljana (Slovenian language) Fourth term: 9th April 2020 –...

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Regulatory workshop: PREPARATION OF DOCUMENTED PROCEDURES FOR MEETING THE REQUIREMENTS OF THE NEW REGULATION IN THE FIELD OF DISTRIBUTION OF MEDICAL DEVICES

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On 25/03/201921/02/2020By rapharmIn Current educations and trainings, Regulatory news, Uncategorized

Additional term: Date to be determined raPHARM premises, Miklošičeva 30, Ljubljana (Slovenian language) Regulatory workshop PREPARATION OF DOCUMENTED PROCEDURES FOR MEETING THE REQUIREMENTS...

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Regulatory seminar and workshop on medical devices: NEW LIABILITIES AND RESPONSIBILITIES OF DISTRIBUTORS OF MEDICAL DEVICES IN THE EU – Why to review current agreements?

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On 25/09/201819/10/2018By rapharmIn Current educations and trainings, Regulatory news, Uncategorized

27th & 28th November 2018 Radisson Blu Plaza Hotel Ljubljana (Slovenian language) Regulatory seminar and workshop on medical devices NEW LIABILITIES...

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International regulatory seminar and workshop: NEW EU LEGISLATION EFFECT ON MEDICAL DEVICES DISTRIBUTORS’ LIABILITIES

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On 20/09/201820/09/2018By rapharmIn Current educations and trainings, Regulatory news, Uncategorized

29th & 30th November 2018 Radon Plaza Hotel Sarajevo, BIH (Croatian-Serbian-Bosnian-Montenegrian jezik) International regulatory seminar and workshop NEW EU LEGISLATION EFFECT ON MEDICAL...

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Educational conference: PACIENT SUPPORT PROGRAM – WHAT IS ALLOWED IN THE EU AND WHAT IS NOT?

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On 19/09/201819/10/2018By rapharmIn Current educations and trainings, Regulatory news, Uncategorized

26th November 2018 Radisson Blu Plaza Hotel Ljubljana (Slovenian language) Educational conference PACIENT SUPPORT PROGRAM – WHAT IS ALLOWED IN THE EU...

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Regulatory seminar: HOW PREPARED ARE YOU FOR NEW MEDICAL DEVICES REGULATION?

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On 06/03/201827/03/2018By rapharmIn Current educations and trainings, Regulatory news

10th May 2018 Radisson Blu Plaza Hotel Ljubljana (Slovenian language) Regulatory seminar: HOW PREPARED ARE YOU FOR NEW MEDICAL DEVICES REGULATION?...

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Regulatory conference ETHICS IN REGULATORY AFFAIRS FOR MEDICINAL PRODUCTS AND MEDICAL DEVICES

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On 20/02/201821/02/2018By rapharmIn Current educations and trainings, Regulatory news, Uncategorized

25th & 26th April 2018 Radon Plaza Hotel Sarajevo (Serbo-Croatian-Bosnian-Montenegrian language) Regulatory conference ETHICS IN REGULATORY AFFAIRS FOR MEDICINAL PRODUCTS AND MEDICAL...

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About raPHARM

raPHARM is a consultancy and education office specialising in pharmaceutical and medical devices regulatory affairs. The office was founded by Ms Vesna Koblar, MD. PhD., an internationally recognised expert in this area with extensive experience and knowledge.

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