

Community of Experts
High levels of compliance are vital to the credibility of and public trust in life science R&D. Enhancing community members’ knowledge supports the goal of our industry – improving the health outcomes of all.
Controlled substance legislation has changed rapidly in recent years as legislators respond to the issues and concerns in society. For example, enhanced suspicious order monitoring requirements in response to the opioid epidemic, and ‘super generic’ definitions in response to the rapid increase in synthetic cannabinoid analogs in the mid-2010s. Remaining compliant in this environment is an ever-growing challenge, and consequences for breaches are severe.
Cross-Border Shipping legislation is also a very dynamic environment and ties in very closely with aspects of Controlled Substance logistics. Since the start of the pandemic there have been many additional challenges in moving Pharmaceutical R&D materials. Our members must ensure shipments are fully compliant with all national and international requirements. There is no leeway in making mistakes as delayed or rejected shipments could have a tremendous negative impact on pharmaceutical development timelines.
Jack DeCicco
EHS Manager Hazardous Substances and Shipping Lead
GlaxoSmithKline
Terry Richard Stouch, PhD
CSO / Senior Editor-in-Chief
Science For Solution, LLC / Springer Nature “Journal of Computer-Aided Molecular Design”
Andreas Schumacher
Head of Operational Compliance
Novartis Pharma AG
Joseph Pease (Joe)
Analytical Research, Discovery Chemistry
Genentech
About Jack:
Jack joined GSK in 2006. In his current position he is leading a global team of Shipping Compliance Managers. Jack holds a BA in Economics from Ohio University.
Why are you part of the CSCS expert community?
This community is wonderful way to keep current with relevant Research and Development controlled substance legislation around the world.
What is the biggest challenge for you in CS compliance?
Interpretation of vague regulations.
About Terry:
For 30 years Terry has been designing the function as well as the structure of small molecule drugs at length with Bristol-Myers Squibb, Lexicon Pharmaceuticals, and several others by using ever advancing computational methods and experimental understanding of biological “targets and functional results.
Why are you part of the CSCS expert community?
To be informed of the legal complexities of the attempts to equate different molecules without results of detailed biological experiments. To provide information about these differences to pharmaceutical companies.
What is the biggest challenge for you in CS compliance?
To make the point that even very small differences between 2 molecules – even one atom change – can result in very different biological results.
Andreas joined Novartis in 2013. In his current position he is leading a global team of experts in controlled substances, trade and human tissue compliance at the Novartis Institute for Biomedical Research (NIBR).
Prior to joining Novartis, Andreas completed his postdoctoral research at Harvard University. He holds a Ph.D. in chemistry from the University of Basel, Switzerland.
Why are you part of the CSCS expert community?:
The CSCS expert community is a unique opportunity to discuss and share best practices in the area of controlled substances regulations with peers in the pharmaceutical industry.
What is the biggest challenge for you in CS compliance:
To keep up with the constantly changing world-wide country-specific CS legislation and the associated risk of a broad definition for a new class of generics.
Joe joined Genentech in 2011 where he leads the Analytical Research team in Discovery Chemistry. Prior to joining Genentech, Joe worked at Roche Palo Alto and held leadership positions in both research and informatics. Joe earned a Ph.D. in Chemistry from the University of California, Berkeley.
Why are you part of the CSCS expert community?
The CSCS expert community is a unique opportunity to learn, discuss, and share best practices in the area of controlled substances regulations with peers in the pharmaceutical industry.
What is the biggest challenge for you in CS compliance?
Keeping up with the constantly changing regulations in order to identify controlled substances by chemical structure.
Jessie Bin Song
Director, Controlled Substance Compliance
Merck
Joe Bradley
Chief Executive Officer
Scitegrity Limited
Karl Cable
Manager, Radiation and Controlled Substances UK
GlaxoSmithKline
Nicolas Fur
Novartis Institute for Biomedical Research
Jessie joined Merck in 1996. In her current position she is leading company’s controlled substance compliance program worldwide supporting all business divisions. Jessie holds a BA in Chemical Engineering.
Why are you part of the CSCS expert community?
This community provides an open and safe environment for the members to benchmark and share experience in various areas of focus related to controlled substance legislation and regulations around the world. The community works as a team to tackle the challenges and strive to stay current with the changing environment.
What is the biggest challenge for you in CS compliance?
Stay current with the changing requirements and define an effective and efficient approach to maintain compliance.
I co-founded Scitegrity, the developers of Controlled Substances Squared and ExpediChem in 2011. Prior to this, after completing my degree in Biochemistry from the University of Warwick, I worked for over a decade in drug discovery, screening and compound logistics at companies such as Pfizer and AstraZeneca, covering both lab and informatics based roles.
Why are you part of the CSCS expert community?
The CSCS expert community has provided and driven improvements and solutions to long standing challenges relating to controlled substance compliance. Prior to its existence, those tasked with the practical aspects of implementation had very little support, information and tools to help them. Now, through its efforts and those of its members, increasingly legislators are understanding how modern drug discovery works and are discussing how changes to the laws relating to chemical regulation and controlled substances can help with this.
What is the biggest challenge for you in CS compliance?
Where there is ambiguity in legislation, trying to get meaningful and timely engagement from regulators to understand exactly what they mean and how this applies to scientific research.
Karl joined GSK in 1988 (at Glaxo Group Research, Greenford, London). He worked as a radiochemist for many years and was involved in the preparation of drug candidates labeled with radioactive and stable isotopes. In his current position, he leads controlled drug compliance and all aspects of radiation protection (ionising and non-ionising) for GSK R&D in the UK. Prior to joining GSK he studied at the University of Leeds. He holds a Ph.D. in chemistry from the University of Leeds, UK.
Why are you part of the CSCS expert community?
CSCS has proved to be a valuable forum for gathering and sharing intelligence on controlled substances. It has enabled the research sector to develop shared solutions to emerging issues in CS compliance. This is particularly important when new legislation contains ambiguities that are open to interpretation.
What is the biggest challenge for you in CS compliance?
Keeping up with developments and obtaining advanced knowledge of new CS legislation worldwide. Gaining an understanding of how regulators operate and devise new approaches to CS compliance.
Nicolas joined the Novartis Institute for Biomedical Research (NIBR) in 2008 and worked for a decade in medicinal chemistry on multiple projects and technologies. I joined the NIBR controlled substances compliance team in 2019.
Why are you part of the CSCS expert community?
CSCS is a great opportunity to be exposed to various legislations and share best practices with peers. It has benefited the pharmaceutical industry by acting as a common voice and interlocutor with regulation agencies enabling major achievements.
What is the biggest challenge for you in CS compliance?
Keeping up with constantly changing regulations and engage with regulators to understand how they operate and what is the future.
Akos Papp
Product Manager of Compliance Checker and cHemTS
Chemaxon
Akos joined Chemaxon in 2007, and was the Product Owner of several chemical software solutions. In his current position, he is the Product Manager of Compliance Checker and cHemTS. Prior to ChemAxon he has always worked in the chemoinformatics area, both in the software development and in the drug design field. He holds an MSc in Chemical Engineering from the Technical University of Budapest, Hungary.
Why are you part of the CSCS expert community?
The CSCS community provides an opportunity to meet experts working on this field and act together. We can discuss the challenges posed by the latest regulation updates, and as a community we can contact the regulatory bodies to get clarifications or we can even suggest modifications.
What is the biggest challenge for you in CS compliance?
The proper translation of the wording of regulations to the appropriate (sub)structural queries, which is the key in the accurate detection of controlled substances.