Our consultants translate science and regulation to determine best approaches to testing, registration, and marketing of EPA, FDA, and International antimicrobial/pesticide products. SRC goes one step further ensuring that those products can be brought to market not only in the United States and its territories but also internationally.
Organized and creative science professional using proven skills in microbiology, antimicrobial technology, research, project management, product development, industry and government alliances. Available to respond to the needs of the antimicrobial industry and related disciplines. Qualified by over thirty years of comprehensive experience in the antimicrobial, biotechnology, healthcare, and pharmaceutical industries.
VP, REGULATORY SERVICES
Customer driven, diligently striving for creative solutions for problem solving situations. Extensive background in numerous functions of product testing, registration, and marketing. Qualified by over forty years of experience and professional growth in the various aspects required to bring products to market.
VP, REGULATORY SERVICES
Hard-working, scientific oriented professional with over eighteen years of laboratory experience and EPA/FDA regulated manufacturing production and supervision. Proficient in federal EPA and state antimicrobial and insecticide pesticide registration preparation and required data development. Expertise in various laboratory technologies and equipment including Agilent and Waters HPLC, gas chromatograph, FTIR and computer systems. Trained in document control of GMP, GLP and FDA regulated records.
ASSISTANT FEDERAL TEAM MANAGER
Tony’s science education provides the detail-oriented foundation required to manage various aspects of federal EPA antimicrobial and insecticide pesticide registrations, preparation, and required data development. In addition to many of Tony’s consultant responsibilities, he monitors California and EPA regulations and is an integral part of label reviews.
PRINCIPAL REGULATORY CONSULTANT
Brings over ten years of industry experience and perspective in federal EPA, state and Canadian antimicrobial registration. Prepares and executes projects, from data development and submission to post-market maintenance, with great attention to detail and organizational skills. Contributes strategy and current regulatory concerns to diligent preparation of antimicrobial applications. Proficient GLP-trained auditing skills.
With over fifteen years of experience in EPA FIFRA, Health Canada, DFE, Safer Choice, OMRI, WoolSafe and NSF compliance, Jamie is the perfect fit to assist you in advancing your product from research and development to retail. She is currently a member of the GreenBlue CleanGredients Advisory Committee and HCPA Antimicrobial Division Membership Committee.
Denise Burnside, Ph.D.
Denise’s experience includes over twelve years of scientific research experience that has resulted in her contribution to the field of microbiology through both publications in peer-reviewed journals and presentations at scientific conferences. Her attention to detail and extensive background in microbiology provides the firm foundation required to facilitate the development of product efficacy data for the EPA registration of antimicrobial products.
Megan brings 12 years of experience working within the contract laboratory and regulated product development industry. She has gained extensive knowledge in EPA and FDA Good Laboratory Practice regulations, and garnered comprehensive expertise in quality assurance. She successfully manages and analyzes process developments, skillfully executes project coordination, and continuously drives quality improvement efforts while ensuring full compliance with regulations. Her amassed range of experience in these areas provides the attributes necessary to assist in navigating your product through R&D to registration.
Becky’s education and her 15 years’ experience in the contract laboratory space has provided her with the knowledge and expertise in GLP, GMP, GDP, project management, methodology, and efficacy study execution. She is currently a member of HCPA, ASTM, ASM, and SQA. Becky has a firm technical understanding of efficacy methodology and can help you with your raw data and report review, protocol development, and study management.
STATE REGISTRATION MANAGER
Rene’s management background and her willingness to assist with whatever needs done has proven her to be an extraordinary mentor and respected state registration team member. Her strong commitment to excellence gives SRC clients the service they have come to expect in all facets of product registration.
Celeste’s biology background, naturally inquisitive nature, and thorough research skills have helped prepare her for the analytical world of state-specific pesticide regulations. She strives to assist in any capacity possible during the registration process of every client who comes to SRC seeking scientific and regulatory guidance.
Chelsey’s background in regulatory and compliance along with her continuing education in Business Management brings a resourceful perspective to SRC. Keen to jump in and help where needed helps our team to meet goals and surpass expectations.
Michelle’s professional background in clinical research and quality control in tandem with her commitment to exemplary customer service entrusts clients receive knowledgeable, current and forward thinking service. Her knowledge of scientific techniques provides a strong foundation as Michelle navigates through the state registration process.
With Michelle’s customer service background and management education, she is a trusted business partner. She provides daily hands-on service to clients, offering timely, creative solutions to their needs. She is enthusiastic, accessible, and works collaboratively to achieve goals.
Tom’s mathematical background and problem solving ability provide a solid foundation for the detail oriented procedures involved in the state registration process. His teaching experience and communication skills enable him to work cooperatively with multiple shareholders to meet clients’ needs.
Responsible for business aspects of our dynamic work environment including finances, legal, scheduling, procurement, and organization. Over thirty years’ experience in filing of state and federal EPA registrations. Creative, multi-task oriented, excellent oral and written communication skills.
OPERATIONS TEAM MANAGER
Lisa brings over fourteen years of management experience to SRC. She is a focused, customer driven professional with excellent attention to detail and exceptional communication skills. Her strong commitment to excellence gives SRC clients the service they have come to expect.
Cassie is responsible for analyzing and increasing efficiencies in our business practices. Her customer service and risk management experience provide a unique perspective to our Operations Team. Her creativity and problem-solving skills are used daily to help the SRC team provide the best possible service to our clients.
Andrea assists in increasing team efficiencies by giving support both operationally and administratively. Having a positive attitude and proactive approach to work, she is able to provide assistance in meeting our clients’ needs.
Scientific & Regulatory Consultants, Inc. co-founder Sally Hayes passed away December 27, 2018.
Sally enjoyed a successful 35-year career in the antimicrobial industry and was a wonderful mentor, friend, role model, and trusted business partner. Her brilliant, creative, and tenacious regulatory skills helped her to form lasting relationships with regulators, laboratories, trade associations, and clients which was critical to the success of SRC. She was a member of numerous industry groups, supported many local community organizations, and established The SRC Scholarship Endowment to help local students realize their dreams of a science education.
We cherish the years spent together preparing submissions, crafting positions, revising standards, and shepherding products to market.