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Pass Every Inspection

Compliance For Your Daily Operations

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At Lifecycle Technologies, we help your company set up strict protocols to ensure you produce safe, quality products.

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If you are looking for a new career, take a moment to learn more about us and our innovative, experienced team.

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Make sure your biotech or pharmaceutical company stays on the right side of the law by studying the current regulations.


Find all the information you need in this list to better understand important government guidelines and procedures.


Make sure your company follows the regulations
with the help of one of our our compliance consultants.

Call (732) 795-0835

About Us

Lifecycle Technologies, a compliance consulting firm based in Brielle, New Jersey, provides a wide variety of services to help pharmaceutical and biotech companies meet international and federal regulatory requirements. Since 1995, our team has specialized in helping companies develop efficient and cost-effective quality systems that pass audits and inspections so that they can produce high-quality products.

Coming strictly from a biopharmaceutical background, our consultants have worked successfully with many traditional pharmaceutical, and biotech clients. We are not a massive, faceless firm, so you can rest assured you will work directly with our knowledgeable and experienced consultants through the entire process.

Our Services

Global Deployment | Compliance Consulting | GMP/GLP Auditing | Warning Resolution | GMP Quality Systems | CSV | GMP Qualification | GMP Process Validation | Facility Design | GMP Utility Design | Program Management | IT Implementation | Training | Management Consulting

Contact Us

Thank you for your interest. For questions or comments, please use the information listed here. We look forward to hearing from you soon.

Brielle, NJ 08730

Hours of Operation
Monday - Friday, 8 a.m.-5 p.m.
Additional Hours Available Upon Request

Service Area
Serving Clients in North America & the European Union

(732) 795-0835 (Office)

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