Life sciences teams
For drug, biologic, medical device, diagnostic, digital health, consumer health, and other life sciences teams sourcing external regulatory input or project support.
About RegSeek
Building a more controlled way to access and engage external regulatory affairs expertise.
RegSeek helps life sciences teams obtain focused regulatory input and confidentially source, compare, and engage regulatory consultants, specialist advisors, subject-matter experts, and firms.
Why RegSeek exists
External regulatory needs are too sensitive for generic outreach.
Life sciences teams often need external regulatory expertise for sensitive, time-critical, or market-specific work: product strategy, submissions, market entry, labeling, CMC, clinical evaluation, technical documentation, or specialist review.
Traditional sourcing relies on referrals, public searches, and broad outreach. That can force teams to share sensitive context before they know whether a provider has the right expertise, availability, or fit.
RegSeek is built to make external regulatory support more structured and controlled: get focused input for defined questions, or compare relevant providers and choose how to engage when broader project support is needed.
Who RegSeek is for
Built for fit-sensitive regulatory sourcing.
RegSeek is designed for teams and providers who need a more structured way to find, compare, and engage external regulatory expertise.
Regulatory and commercial leaders
For regulatory affairs, commercial, market-access, and launch leaders who need specialist expertise, market coverage, or temporary capacity for defined workstreams.
Business development, licensing, and diligence teams
For BD, licensing, corporate development, investor, and M&A teams that need regulatory pathway, approval-readiness, market-access, or transaction-risk input.
Consultants and firms
For qualified regulatory consultants, expert advisors, and firms seeking buyer requests matched to their expertise.
How RegSeek is different
Designed around confidentiality, context, and fit.
RegSeek is not a generic freelancer marketplace, public expert directory, staffing agency, or broad consulting listing. It is built around the specific needs of regulatory affairs sourcing in life sciences. See how RegSeek supports focused input and provider sourcing →
Confidential by design
Requests can be structured and masked before provider review so sensitive details are not exposed too early.
Vetted provider profiles
Provider participation can be vetted by regulatory focus, service categories, market coverage, relevant experience, and fit with RegSeek's participation requirements.
Structured comparison
Buyer teams can compare providers by expertise, market fit, availability, service category, and request relevance.
Controlled path to engagement
Buyers control when identities are revealed and can choose direct contracting or RegSeek-supported structured setup where available.
Vetting and governance
What sits behind vetted participation.
Trust on RegSeek is supported by structured review and governance, not claims alone. These review layers operate behind every request, profile, and engagement.
Provider vetting review
Provider profiles are reviewed before buyer-facing publication, with verification and a verified badge on approval. Representative experience can be anonymized.
Structured regulatory taxonomy
Providers are represented by product type, market coverage, service categories, experience level, languages, and availability — so buyers compare regulatory fit, not generic profile keywords.
Request and interest moderation
Confidential requests, expressions of interest, and advisory briefs are supported by admin review workflows before they move between buyers and providers.
Advisor compliance screening
Advisors participating in Written Regulatory Advice and Regulatory Expert Calls go through employer disclosure preferences, conflict-of-interest screening, and restricted-topic controls.
Controlled payments
Shortlist & Connect and paid RegSeek services use Stripe-backed checkout or invoicing, with pricing confirmed before payment.
About the founder
Built from both sides of regulatory sourcing.
RegSeek was founded by Fred Sim, a regulatory affairs professional and registered pharmacist with more than a decade of experience across pharmaceuticals, biotechnology, and medical devices in APAC and international markets.
In regional regulatory roles at multinational pharmaceutical companies, Fred identified external expertise needs, engaged consultants and partners, and managed the resulting work. He has also worked on the provider side through CRO and independent consulting engagements covering regulatory strategy, submissions, and lifecycle management across multiple markets.
Seeing the process from both sides showed how difficult it can be to identify suitable expertise consistently, share enough context to assess fit, and move into the right engagement without exposing sensitive information too early.
Fred founded RegSeek to create a more structured and controlled approach for life sciences teams to obtain focused input on defined regulatory questions, source suitable providers for regulatory work, and choose the right path to engagement.
Fred is based in Singapore. Connect with Fred on LinkedIn.
Early access
Help shape a more controlled way to find and engage regulatory expertise.
RegSeek is currently preparing early access for selected buyers, providers, advisors, and firms. Join the appropriate early-access path so RegSeek can review your role, use case, market focus, and timing.