Karandeep Singh Badwal Email & Phone Number

Do you need help legally bringing your medical device to market in the UK, EU or USA? Feel free to send me a message to see how we can work together on achieving this 📧Using my extensive knowledge of scientific, legal and business issues acquired throughout different aspects of my work, my main role is to ensure the appropriate licensing, marketing and legal compliance of medical devices to make sure that they reach the end consumer safely. I see myself as a crucial link between the industry and the general public; as their bridge of trust to ensure that the medical products that they use are of a high quality standard and meet every guideline there is. Moving forward, I am always willing to meet people from both the medical and healthcare industry to share their experiences and stories. If you take an interest to what I do or wish to contact me for business and/or other opportunities, please feel free to connect with meBook a Microconsulting call with me: https://calendly.com/karandeepbadwal/microconsultingFunctional Areas of Focus:- Medical Devices (ISO 13485, ISO 14971, MDR, Quality Management Systems, Technical File Remediation, ISO 11607, ISO 14644, IQ OQ, PQ, FDA CFR 21, GMP, 510k, IEC 62304, IEC 82304, Complaint Handling, CAPA, Sterilisation, Software Validation, Computer System Validation CSV, eQMS, Article 10(9)- Regulatory Affairs (RA)- Quality Assurance (QA/QC)- Medtech (SaMD, Digital Health, Artificial Intelligence/AI, Machine Learning)- PRRC (Person Responsible for Regulatory Compliance) - UKRP (UK Responsible Person)- eQMS (Qualio, Greenlight Guru, JIRA, Atlassian, G Suite, Confluence, Mastercontrol)- Certified ISO 13485 QMS Auditor (CQI/IRCA)- Certified EU MDR Practitioner (CQI/IRCA)- UKCA, CE, FDA, 510k, PMA, De NovoMy Content:- How to build an ISO 13485 Quality Management System: Tinyurl.com/yagnzxm7- ISO 13485 or ISO 9001 Quality Management Systems: Tinyurl.com/yavjg6kq- Medical Device CAPA (Corrective Action and Preventative Action): Tinyurl.com/ycqubsba- ISO13485 V FDA CFR 21 Part 820: Tinyurl.com/y94bkf5w- How To Obtain A European CE Mark: Tinyurl.com/yxzplrr2- What is UKCA and UKRP: Tinyurl.com/cus6teyy - What is an EC REP: https://tinyurl.com/59durub8Follow me on YouTube @KarandeepBadwalFollow my Podcast @The MedTech Podcast: https://open.spotify.com/show/32CvtseLj3KknqYDFdO7P3

Listed skills include Regulatory Affairs, Science, Pharmaceutical Industry, Analytical Chemistry, and 48 others.