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Christine Woods is a Vice President, Regulatory Affairs at Conventus Biomedical Solutions, Inc. at Conventus Biomedical Solutions, Inc.. They possess expertise in regulatory affairs, pharmaceutical industry, fda, drug development, oncology and 31 more skills.
Conventus Biomedical Solutions, Inc.
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Vice President, Regulatory AffairsConventus Biomedical Solutions, Inc. Apr 2020 - PresentSan Diego, California, UsBranded / Ethical Drug Development - Oncology [Tablets, Capsules], Oncology [Cell Therapy Parenterals], Gastroenterology [Tablets, Capsules], Dermatology [Tablets, Capsules], Dermatology [Cell Therapy Parenterals], Neurology [Cell Therapy Parenterals], Medical Devices, Initial INDs, Original NDA, IND/CTA/CTX Maintenance, Drug & Device Annual Registrations and Listings -
Sr. Director, Regulatory AffairsConventus Biomedical Solutions, Inc. Mar 2019 - Apr 2020San Diego, California, UsBranded / Ethical Drug Development - Oncology [Tablets, Capsules], Oncology [Cell Therapy Parenterals], Gastroenterology [Tablets, Capsules], Dermatology [Tablets, Capsules], Dermatology [Cell Therapy Parenterals], Neurology [Cell Therapy Parenterals], Medical Devices, Initial INDs, Original NDA, IND/CTA/CTX Maintenance, Drug & Device Annual Registrations and Listings -
Global Regulatory LeadPuma Biotechnology, Inc. Nov 2011 - Nov 2018Los Angeles, Ca, UsBranded / Ethical Drug Development - Oncology [Tablets, Capsules]Initial INDs/CTAs/CTXs, original MAA & NDAe.g. NERLYNX® (neratinib maleate) -
North American Regulatory LeadJanssen Inc. Feb 2009 - Nov 2011Toronto, Ontario, CaBranded / Ethical Drug Development - Oncology [Tablets, Capsules]Initial INDs/CTAs/CTXs, original MAA & NDAe.g. ZYTIGA® (abiraterone acetate) -
Associate Director, Regulatory AffairsWatson Pharmaceuticals, Inc. (→ Actavis → Allergan) Sep 2002 - Jan 2009Generic Drug Development [Tablets, Capsules, Nasal Sprays, Inhalation Aerosols, Injectables, IVs, Transdermal Patches; Gels, Topical Gels, Lotions; Creams, Buccals]Original ANDAs (mostly Paragraph 4s)
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Director, Regulatory AffairsPain Therapeutics, Inc. Apr 2000 - Sep 2002Branded / Ethical Drug Development - Combination Drug Products for the Treatment of Pain [IVs, Tablets, Capsules]Initial INDs/CTAs/CTXs
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Manager, Regulatory AffairsAradigm Corporation Jun 1996 - Apr 2000Branded / Ethical Drug Development - Combination Drug Products for Delivery as Pulmonary Aerosols [Combination Drug/Electromechanical Device; Combination Biologic/Electromechanical Device Products Submitted to FDA as Drug Products for the Treatment of Pain, Diabetes, Cystic Fibrosis, etc.]Initial INDs/CTAs/CTXs & 510ke.g. AERx® & SmartMist™
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Regulatory Associate, Sr. Analytical Chemist, Analytical ChemistCygnus Therapeutic Systems (Cynus Research Corp.) Feb 1989 - Jun 1996Branded / Ethical Drug Development - Transdermal Drug Products [Hormone Replacement Therapy, Birth Control, Pain Therapy, Smoking Cessation, etc.]Initial DMFs, initial INDs/CTAs/CTXs, original NDAse.g. FemPatch™, Nicotrol® Transdermal & Ortho Evra®
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Analytical ChemistLiposome Technology, Inc. Jun 1988 - Feb 1989Branded / Ethical Drug Development - Liposomal Drug Products[Injectables for Oncology, Infectious Diseases, etc.]e.g. DOXIL® (doxorubicin hydrochloride liposome) Injection
Christine Woods Skills
Christine Woods Education Details
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Dominican University Of CaliforniaBiology / Chemistry -
San José State UniversityToxicology
Frequently Asked Questions about Christine Woods
What company does Christine Woods work for?
Christine Woods works for Conventus Biomedical Solutions, Inc.
What is Christine Woods's role at the current company?
Christine Woods's current role is Vice President, Regulatory Affairs at Conventus Biomedical Solutions, Inc..
What is Christine Woods's email address?
Christine Woods's email address is wo****@****aol.com
What schools did Christine Woods attend?
Christine Woods attended Dominican University Of California, San José State University.
What skills is Christine Woods known for?
Christine Woods has skills like Regulatory Affairs, Pharmaceutical Industry, Fda, Drug Development, Oncology, Regulatory Submissions, Gmp, Ind, Biotechnology, Clinical Trials, Sop, U.s. Food And Drug Administration.
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