Happy with

Happy Scientifics Limited ®

Peddy Adhyaksa

CEO, Viorez Medizintechnik GmbH Munich Germany

Viorez Medizintechnik GmbH has utilized Happy Scientifics Ltd to our organization since 2021. Dr. Siddiqul Haque has provided both regulatory and clinical expertise to ensure that performance evaluations for new products are undertaken to meet CE marking and other regulatory jurisdictions and has also been invaluable in creating /reviewing and approval of technical documents. Happy has also provided regulatory support to our company, including gap analyses of product and preparing complete technical file including clinical evaluation report with literature search according to EU MDR.

Dr. Siddiq is a very experienced and knowledgeable clinical, regulatory and quality professional and works to the highest quality standards. He has an outstanding ability to turn underperforming device companies into compliant and effective businesses. Dr. Siddiq was able to quickly identify the major compliance issues and translate this into a working improvement plan based on the main compliance risks balanced with a desire for long term quality and regulatory improvement. Ultimately the plan was delivered and the business continued to develop and improve in key quality and regulatory compliance areas. I would recommend him as a highly experienced and capable Clinical, Quality & Regulatory Leader. I am confident in Dr. Siddiq’s abilities to provide support for any IVD/medical device regulatory, clinical or quality requirements.

Mohammed Adil

Regulatory Manager, Immunodiagnostic System UK

“As a professional who has worked closely and managed several projects of Dr Siddiqul Haque during my tenure in HCL Technologies Limited, I can confidently attest to his technical proficiency, vast knowledge, and excellent managerial skills. His ability to analyze and synthesize complex information, combined with his attention to detail, has enabled him to develop comprehensive clinical evaluation reports, performance evaluation reports and tech files that meet regulatory requirements.

He has a unique talent for navigating the complex and ever-changing regulatory landscape for medical devices, which has proved invaluable to our clients during the transition from MDD to MDR and IVDD to IVDR. He has helped our clients remain compliant with the latest regulations, ensuring the timely and successful launch of several new medical devices.
Furthermore, Dr Siddiqul Haque has demonstrated excellent managerial skills in leading project teams and collaborating with cross-functional teams. His ability to communicate effectively and establish strong working relationships has made him a valuable team member and a trusted advisor to senior management.
Overall, I highly recommend him for any organization in need of a CER/PER Writer, Tech File Remediation Specialist, MDR and IVDR Transition Specialist. He is a consummate professional with a wealth of knowledge and expertise that will undoubtedly bring value to any team or organization.”

Ava women Swiss
ENTE CERTIFICAZIONE MACCHINE Italy
Eurofins Europe
Iskra Mdical Slovenia
Baxter International Inc. US
JRI Orthopaedics UK
LivaNova Italy
MISS Mediyintechnik, Berlin
mPOR Slovenia
North American Science Associates
Merz North America, Inc.
Elquent Life Sciences
Orthofix, US
SQA SERVICES, INC., US
KLIFOVET AG Munich
SureScreen Diagnostics, UK
VALIDANT Ireland
Agilent Technologies Singapore
VIOREZMED Munich
VITROS ENS Turkey
Carl Zeiss Germany

Peddy Adhyaksa

CEO, Viorez Medizintechnik GmbH Munich Germany

Viorez Medizintechnik GmbH has utilized Happy Scientifics Ltd to our organization since 2021. Dr. Siddiqul Haque has provided both regulatory and clinical expertise to ensure that performance evaluations for new products are undertaken to meet CE marking and other regulatory jurisdictions and has also been invaluable in creating /reviewing and approval of technical documents. Happy has also provided regulatory support to our company, including gap analyses of product and preparing complete technical file including clinical evaluation report with literature search according to EU MDR.