PI's Krystal Santiago (VP Regulatory Affairs) discusses the shift towards point-of-care diagnostics and its drive to reduce test times while meeting stringent regulatory standards. Learn more about PI's regulatory expertise here: https://lnkd.in/dZKT6g2n #FDA #productdevelopment #regulatoryadvice #regulatorystrategy #regulatorystandards
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Continuing with our Qmed Strategic Consulting introduction.... meet Claudia Argenti! We love having Claudia on the team and she helps keep us all up to date with the last news in regulatory affairs! #Qmed #MedicalDevices #RegulatoryAffairs #ClinicalAffairs
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Ensuring your trial adheres to regulatory and safety standards is essential for having a successful clinical trial. In the June Issue of PharmaTimes Media Ltd Magazine, Mai Mishir and David Turner, our regulatory and safety experts, share insights on how to maximize success. Read the article: https://hubs.la/Q02yJrGw0 #Safety #Regulatory #ClinicalTrials #ClinicalResearch
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Ensuring your trial adheres to regulatory and safety standards is essential to having a successful clinical trial. In the June Issue of PharmaTimes Media Ltd Magazine, Mai Mishir and David Turner, our regulatory and safety experts shared insights on how to prioritize staying compliant in your trial. Read the article: https://hubs.la/Q02L-dKV0 #Safety #Regulatory #ClinicalTrials #ClinicalResearch
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Streamlining the regulatory maintenance of approved drugs is one way for the biopharma industry to support a balanced approach to drug development and on the mature products that provide the revenues to fund R&D Discover the five key competencies to manage post-marketing regulatory requirements better and more efficiently, in this article by my colleague Moshin Malik – Director, Regulatory Affairs.
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Streamlining the regulatory maintenance of approved drugs is one way for the biopharma industry to support a balanced approach to drug development and on the mature products that provide the revenues to fund R&D Discover the five key competencies to manage post-marketing regulatory requirements better and more efficiently, in this article by my colleague Moshin Malik – Director, Regulatory Affairs.
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Streamlining the regulatory maintenance of approved drugs is one way for the biopharma industry to support a balanced approach to drug development and on the mature products that provide the revenues to fund R&D Discover the five key competencies to manage post-marketing regulatory requirements better and more efficiently, in this article by my colleague Moshin Malik – Director, Regulatory Affairs.
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Streamlining the regulatory maintenance of approved drugs is one way for the biopharma industry to support a balanced approach to drug development and on the mature products that provide the revenues to fund R&D Discover the five key competencies to manage post-marketing regulatory requirements better and more efficiently, in this article by my colleague Moshin Malik – Director, Regulatory Affairs.
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Consultative Development Manager Parexel Biotech at Parexel #neverstopbioteching #clinicaltrials #patientsfirst #globalexpertise
Streamlining the regulatory maintenance of approved drugs is one way for the biopharma industry to support a balanced approach to drug development and on the mature products that provide the revenues to fund R&D Discover the five key competencies to manage post-marketing regulatory requirements better and more efficiently, in this article by my colleague Moshin Malik – Director, Regulatory Affairs.
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Streamlining the regulatory maintenance of approved drugs is one way for the biopharma industry to support a balanced approach to drug development and on the mature products that provide the revenues to fund R&D Discover the five key competencies to manage post-marketing regulatory requirements better and more efficiently, in this article by my colleague Moshin Malik – Director, Regulatory Affairs.
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Streamlining the regulatory maintenance of approved drugs is one way for the biopharma industry to support a balanced approach to drug development and on the mature products that provide the revenues to fund R&D Discover the five key competencies to manage post-marketing regulatory requirements better and more efficiently, in this article by my colleague Moshin Malik – Director, Regulatory Affairs.
