HCPA XPAND2021 Annual Meeting – December 6-9, 2021

HCPA XPAND2021 Annual Meeting - December 6-9, 2021
HCPA XPAND2021 Annual Meeting - December 6-9, 2021

Join us at the HCPA XPAND2021 Annual Meeting  on December 6-9, 2021 in Fort Lauderdale, Florida. A variety of topics will be discussed: public policy and regulatory issues, product registrations, disruptions caused by COVID-19, and much more. Expert-led sessions, for every division and committee, will be held to discuss issues that impact household and commercial products, including ingredient communication, retailer expectations, product safety, supply chain, market trends, packaging, and technical issues.

Melinda and Jeremy will be available throughout this meeting to meet with you and answer any questions you have regarding our regulatory and technical consultancy services.

Melinda Bowman's Picture

Melinda Bowman

Principal Consultant


Jeremy Wilson's Picture

Jeremy Wilson

Principal Consultant


CSI has an established reputation in supporting registration of a range of antimicrobial/biocidal products including disinfectants, sterilizers, preservatives, and unique antimicrobial applications. We support clients introducing their products in European and North American markets through cost-effective strategies.

In the US, we help clients with US Environmental Protection Agency (EPA) and the Food and Drug Administration (FDA) regulated antimicrobial products, as well as State registration management.

In Europe, we assist with active substance approval and biocidal product authorisations to comply with the requirements for the European Economic Area (EEA) (i.e. EU27 plus Iceland, Liechtenstein and Norway). With the new GB BRP regulation now in force for Great Britain, CSI is able to offer GB Article 95 representative support for EU companies.

We also support the global marketplace and have successfully assisted firms with registrations in Canada, Latin America, Asia (China/Taiwan), Australasia, and other geographical markets.

Experienced Support For:

  • Registration Dossier Preparation & Submission
  • Regulatory Strategy
  • Data Review & Evaluation
  • Hazard, Exposure, & Risk Assessments for Human Health & Environment
  • Task Force Management
  • Litigation Support
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Melinda Bowman
Principal Consultant

Expertise: Regulatory Affairs

Melinda has extensive experience in FIFRA regulatory compliance and product registration of agrochemicals and consumer products within the United States and Canada. She provides support and strategy for global pesticide registration actions, including support and coordination of the establishment of international MRLs, FDA 510(k) submissions and hand sanitizer listings.  She specializes in following new developments in regulatory compliance project management for EPA and FDA regulated products as well as agrochemical and pharmaceutical product development. 

B.S., Chemistry, San Francisco State University.

Jeremy Wilson
Principal Business Development Consultant

Expertise: Business Development, Marketing & Regulatory Consulting

Jeremy leads marketing and business development efforts in North America and Latin America. He represents CSI at various industry trade associations and professional societies.

Jeremy has over 23 years of experience in regulatory affairs and product registration compliance with Federal, State, and International chemical regulations. His experience includes government agency interactions and determination of appropriate regulatory pathways to meet product registration objectives. He has prepared numerous registration submissions, placed and monitored necessary Good Laboratory Practice (GLP) studies to develop data and documentation, and served as the primary agency liaison for the registration process. Jeremy has expertise with biorational/biopesticide registration and Latin America regulatory requirements.

B.S., Environmental Science; Minor in Biology, Washington State University.