This coming Tuesday (29.03) at 10.45 a.m. our validation expert Michał Timler will give a lecture about The first stage of implementing a new manufacturing area – good and bad practices during the 13th edition of Spring Pharmaceutical Conference “Efficiency and Optimization” which will be held on 29-30th March in Jachranka near Warsaw. This conference is very
Dear Valued Clients, Partners and Employees, This holiday season, we at eConsulting pause and take advantage of the season to express our gratitude and appreciation to you for cooperating with us. We wish you happy holidays and a year full of happiness and success.
Here it is! A recording from Michał Timler’s presentation at the Swiss MedTech trade fair in Lucerne, Switzerland. In this presentation from Michał Timler, you will hear about the preparation of a Transition Plan and you will be provided with the 12 major steps to be ready for new MDR regulations.
Dear All, In cooperation with our Swiss Partner – Luzern Baar Consulting, we’re delighted to invite you to attend our exclusive webinar session: New reality after MDR implementation – what can you expect? which will take place on June 17 at 11 AM CET. Our expert Michał Timler will cover the
Dear All, It was a pleasure to e-meet you at the Health Tech Regulation – Overview webinar. We’d like to thank you for taking the time to listen to our webinar about MDR timelines, MDCG and Eudamed which we hope you found full of interesting insight. Please find the recording
ecvalidation Team would like to wish all of You Happy Easter!!! May the beauty of Easter holidays warm your heart and bring peace, joy and faith to you and your family.
