News

HCPA Mid-Year Meeting – May 11-13, 2022

HCPA Mid-Year Meeting - May 11-13, 2022

Come join Compliance Services International (CSI) technical and regulatory consultants at the HCPA IMPACT2022 Mid-Year Meeting  on  May 11-12, 2022 in Washington, DC.

From the website:

  • HCPA’s Mid-Year Meeting (MYM), IMPACT2022, is the premier conference to learn about and engage on the public policy issues that impact the household and commercial products industry.
  • Thought leaders from inside and outside the industry will discuss regulatory issues, information related to product registrations, the disruptions caused by COVID-19, and so much more.
  • Every Division and Committee will host expert-led sessions on issues that impact household and commercial products, including ingredient communication, retailer expectations, product safety, the supply chain, market trends, packaging, and technical issues.

Melinda, Jennifer, 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

California

Jennifer Stafford's Picture

Jennifer Stafford

Principal Consultant

Washington State

Jeremy Wilson's Picture

Jeremy Wilson

Principal Consultant

Oregon

Compliance Services International (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
Scroll to Top

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. 

EDUCATION
BS, Chemistry, San Francisco State University.

Jennifer Stafford
Principal Consultant

Expertise: Terrestrial Ecotoxicology, Wildlife Science & GLP Compliance

Jennifer leads or participates in projects related to ecotoxicology, wildlife biology/ecology, GLP Compliance, database management, and USEPA guideline study management. Jennifer’s skills support product registration and regulatory staff, pesticide risk assessment, and endangered species assessments.

Jennifer has 22 years of field research and laboratory ecotoxicology experience, including 16 years of Good Laboratory Practice (GLP) avian and wildlife study directorship and laboratory management. She has extensive experience interpreting the difference between animal behavior in the wild versus in captivity, and how these differences impact study design, husbandry practices and test results.  She has experience with developing and utilizing large data sets and is thoroughly familiar with EPA and OECD regulatory testing guidelines, Good Laboratory Practices guidelines, EPA and OECD guidance on pesticide risk assessment and EPA process for endangered species Biological Evaluation.

EDUCATION
BS, Environmental Biology, Grand Canyon University.
MS, Biology/Ecology, Utah 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.

EDUCATION
BS, Environmental Science; Minor in Biology, Washington State University.