Kaarlo Hentila

Analytical Chemist at Elite Pharmaceuticals, Inc.

Kaarlo Hentila is an experienced analytical chemist with a strong background in pharmaceutical research and quality control. With expertise in various analytical techniques such as HPLC, dissolution, and GC method development, Kaarlo has contributed to the commercial approval of new products and provided support for ANDA filings. Kaarlo's experience includes roles at companies such as Elite Pharmaceuticals, Mondelēz International, and Pfizer/Legacy Wyeth, showcasing a diverse and accomplished career in the pharmaceutical industry.

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Monsey, United States

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Elite Pharmaceuticals, Inc.

Elite Pharmaceuticals, Inc. develops oral sustained and controlled release products. Elite's strategy includes assisting partner companies in the life cycle management of products, to improve off-patent drug products, and developing generic versions of controlled release drug products with high barriers to entry. Elite has four ANDA products partnered with TAGI Pharma; one ANDA has launched, two ANDAs are in the process of a manufacturing site transfer and an additional ANDA is currently under review by the FDA. Elite also manufactures Lodrane D® and receives royalties for Lodrane D®, an allergy product partnered with ECR Pharmaceuticals (“ECR”), a wholly owned subsidiary of Hi-Tech Pharmacal (“Hi-Tech”). Elite’s lead pipeline products, ELI-216, a once-daily abuse resistant oxycodone, and ELI-154, a once-daily oxycodone, are novel sustained release oral formulations of opioids for the treatment of chronic pain, which address two of the limitations of existing oral opioids: the provision of consistent relief of baseline pain levels and deterrence of potential abuse. Elite also has partnered with Mikah Pharma to develop a new product and with Hi-Tech Pharmacal to develop an intermediate for a generic product. Elite operates a GMP and DEA registered facility for research, development, and manufacturing located in Northvale, NJ.