moveproTEC references

  • I have been working exclusively for the life science industries for more than 25 years and have a great deal of experience in the fields of technology, excellence and compliance. On request I proudly provide many satisfied customer references.
  • Amongst others I have exclusively realized customer projects for: 7×4 Pharma, Abbott, AbbVie, Astra Zeneca, Bayer, Boehringer Ingelheim, Cesra, DeLaval, DHL Global Forwarding, Emirates, Ginsana, Kelheim Fibres, Luxair, medac, Merck Serono, Nestlé, NextPharma, Oncotec, Panalpina, SGS, Sweet Ingredients, TAS trust advisory services, TEVA, VTT, Wallenborn, Warner Chilcott, VEIA e.V., Zenith Technologies.
  • Besides compliance upgrades, FDA inspection preparation & remediation projects, I have conducted numerous supplier & site audits (API, excipients, CMO, logistic providers etc.).
  • GMP & GDP basic & advanced training for operators, board members and responsible person, customized QbD training sessions and compliance videos.

moveproTEC presentations

  • „Application of Cold Chain Standards for CRT & Quality Management under GDP”
    ECA conference “Ambient Transport & Cold Chain” 2017, E-Barcelona
  • „GMP Principles & Quality-by-Design”
    EU Project “ModLife – Horizon 2020” Bayer AG 2017, D-Leverkusen 
  • „Quality-by-Design“
    ETH Zurich “Quality & GMP” – Master Study “From Research to Market” 2016, CH-Basel
  • „Application of Cold Chain Standards for CRT & GDP conforming Quality Management”
    ECA conferene “Ambient Transport & Cold Chain” 2016, E-Barcelona
  • „Serialisation & Tamper Proof Seals“
    bdvi Fachtagung bei Romaco Pharmatechnik GmbH 2015, D-Karlsruhe
  • „Falisification Protection & Transparency in Pharma Distribution“
    e-QRM conference “FUTURE – Pharma Supply Chain” 2015, D-Frankfurt
  • „Falsified Medicinal Products“
    VEIA general meeting 2015, D-Berlin
  • „EU GMP guide annex 15 – Transport Verification“
    European Compliance Academy “Annex 15 Conference” 2015, D-Berlin
  • „Quality-by-Design“
    ETH Zurich “Quality & GMP” – Master Study “From Research to Market” 2014, CH-Basel
  • „QbD – faster to market?“
    VDMA general meeting 2014, D-Frankfurt
  • „PAT & QbD – Process Improvements versus FDA”
    10th workshop “process analytics” of GDCh, Endress & Hauser GmbH 2014, D-Gerlingen
  • „GDP – critical review 2010-2014“
    DHL Global Forwarding customer day 2014, D-Leipzig
  • „PAT, QbD, FDA – feedback, feedforward“
    New Lounges 2013, D-Karlsruhe
  • „Continuous Processing – Future of Pharma Production“
    VTT conference “Sense” 2011, FI-Espoo
  • „Pharma 2020 – quo vadis?
    FETTE Pharma Focus 2015, Moderation & lecture, 100 years celebration, D-Schwarzenbeck
  • „Operational & Compliance Excellence – Automation Validation“
    Pharmadule conference “Pharma Summit Ireland” 2010, IRE-Dublin
  • „Risk Management in Pharma Logistics“
    ESN Conference “Cool Chain Logistics” 2010, D-Frankfurt-Mörfelden
  • „Containment or GMP“
    ISPE Workshop “GMP and operator protection” 2009, D-Waiblingen
  • „Lean GAMP – Efficient verification for automated systems“
    SIEMENS Pharmaforum 2009, CH-Muttenz
  • „Process Risk Analysis – regulatory burden or sustainability?“
    FESTO Pharmasymposium 2009, D-Berlin
  • „QbD – Control strategies for containment manufacturing“
    PDA Conference on Quality-by-Design 2008, D-Offenbach
  • „Hygienic zone concepts for high potent drugs“
    Reinraum Lounge & Powder Lounge 2008, D-Karlsruhe
  • „Extended GMP-Training for Labs“
    Service Provider for Pharma Quality Control 2007, Germany
  • „Good Engineering Practice, Quality by Design & PAT“
    FESTO & NNE Pharmaplan Conference on Best Automation Practice 2007, D-Höchst
  • „Qualification, validation, hygiene zones for biotech processes“
    Vienna University Symposium on Recombinant Proteins 2007, D-Wien
  • „Process monitoring for capsule manufacturing under PAT“
    ACHEMA lecture, Frankfurt Fair 2006, D-Frankfurt
  • „PAT process design: Capsules under control“
    APV Seminar Trends und Innovation in der Kapselherstellung 2006, D-Freiburg
  • „PAT solutions for encapsulation processes“
    GDCh expert group symposium on process analytics 2006, D-Berlin
  • „Trends in aseptic filling“
    PDA chapter inauguration meeting Ireland 2006, IRE-Cork
  • Validation of 100% inline leakage testing by HVLD“
    Concept Heidelberg Seminar 100%-Kontrollen Pharma 2006, D-Heidelberg
  • „NIR spectrometry for PAT capsule manufacturing“
    Capsule symposium, Robert-Bosch-GmbH 2005, D-Waiblingen

moveproTEC participation

  • Lectureship at ETH Zurich, Master Study “Pharmaceuticals – From Research to Market”, since 2014
  • Chair of Community of Practice (CoP) on PAT ISPE Affiliate D/A/CH 2008-2013
  • Lectureship at Hochschule Fresenius, Idstein for Master of Science „MSc of Pharmaco-Economics and International Health Economics“ 2012-2014
  • Frankfurt Biotech Alliance (FBTA)
  • Chamber of Pharmacists, Federal State of Hesse (LAK Hessen)

„The exceptional does not happen in ordinary, easy ways."

Johann Wolfgang v. Goethe

„Perspectives in technology, excellence and compliance."

Johann Wolfgang v. Goethe