Emma Louise Jackson, CBiol MSB
Regulatory Specialist

T: +44 (0) 330 223 0615
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BSc, Biomedical Sciences, University of the West of England, Bristol, 2002 (Honors)


Member (CBiol MSB) of the Society of Biology



One of The Acta Group's (Acta®) expert regulatory specialists, Emma Louise Jackson CBiol MSB is distinguished by more than a decade of experience in testing and regulatory environments, assisting clients to achieve regulatory compliance in the European Union (EU), the Americas, and Asia.  She offers particular expertise in worldwide chemical notifications, data analysis, preparing test plans, and managing to completion large and complex compliance projects quickly, cost-effectively, and harmoniously across multiple jurisdictions.  Her focus is on compliance for industrial chemicals and chemical products.

Based in the United Kingdom, Ms. Jackson serves clients in the EU and worldwide.  She offers regulatory advice on the EU Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), Canadian Environmental Protection Act (CEPA), South Korea's Act on Registration and Evaluation, Authorisation and Restriction of Chemical Substances (K-REACH), Taiwan's Toxic Chemical Substances Control Act (TCSCA), Globally Harmonized System (GHS) of Classification and Labeling of Chemicals, and chemical control measures in India, Malaysia, Australia, New Zealand, Japan, and China among others.  Clients rely on Acta specialists such as Ms. Jackson for classification and labeling of substances and mixtures, testing strategy advice, literature searching and reliability assessment, and compilation of regulatory documents, such as IUCLID 5 and Chemical Safety Reports (CSR).  She is an excellent resource for preparation of Safety Data Sheets (SDS) and product labels, as well as liaising with various regulatory authorities.

Representative Engagements:

  • Worked through a complex REACH project for a gas substance by using many different methods including read-across and expert statements to ensure compliance and therefore successful registration.
  • Assisted with testing strategies for substances requiring registration in multiple countries to ensure compliance and therefore successful registration in all jurisdictions.
  • Reviewed existing product labels and SDSs (providing amendments as necessary) to ensure compliance for the EU and worldwide across a broad spectrum of substances, mixtures, and products.


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