RCA provides services to the pharmaceutical, biotech, and medical device industries for the resolution of all compliance, regulatory and technical challenges.
PDA Annual in Long Beach CA has officially started! Come by booth 430 to learn how we can help you with your regulatory, quality, compliance and Lab Testing needs.
#PDAweek
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We are 2 weeks away form the 2024 PDA Annual meeting in Long Beach CA! Stop by booth 430 during the event or click below to learn how RCA can help you with all of your regulatory, compliance, quality and laboratory testing needs.
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Click below to read about RCA's regulatory compliance consultants as they discuss FDA investigation timelines and compliance risks.
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Click below to hear from RCA's medical device consultants on how to understand risk management for machine learning in medical devices.
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Click now to learn how each RCA quality consultant uses the 5 Why's for effective root cause determination & preventing future problems.
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Click to learn how each RCA pharmaceutical consultant approaches supply chain management and helping clients avoid interruptions.
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Follow the link below to learn how RCA regulatory compliance consultants address differences between regulatory compliance & real compliance.
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Follow the link to read as RCA's pharmaceutical consultants provide simple answers to root cause analysis regarding deviation investigations.
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Happy New Year! We want to thank you all for a great year in 2023 and we all are looking forward to 2024. #SafegaurdingGlobalHealth
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Click now to learn more from RCA's pharmaceutical consultants about microbial process design & how to improve your contamination control.
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Join us and our friends at @Sterigenics1 and @NelsonLabs for this FREE webinar where we will discuss laboratory testing and terminal sterilization considerations and steps to help ensure compliance with regulatory requirements within the US and EU.
https://t.co/ptgzZI5meV
Happy Thanksgiving! This year, we are thankful for all the amazing people in our organization as well as our client's organizations. From our family to yours, wishing you a wonderful Thanksgiving! 🦃 #thanksgiving
Learn more from RCA's regulatory compliance consulting team in this published article about emerging therapies & cell and gene innovation.
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Click to learn from RCA's regulatory compliance consultants about 21 Code of Federal Regulations (CFR) Parts 210 and 211 for managing remediation & quality assurance expenses. Link below ↓
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Follow the link below to learn from RCA's pharmaceutical consultants as they discuss ALCOA and Data Integrity elements to avoid FDA regulatory citations.
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Learn more about how Data Integrity contributes to the reliability, consistency, and accuracy of data at rest and in transit. Link Below ↓
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Learn how to achieve more successful testing outcomes by attending this Nelson Labs seminar in San Jose, California, November 7th - 9th. RCA's Eric Januszewski will be covering FDA Inspection Readiness and how to prepare your teams.
https://t.co/ir4FXGJmHE
Click to learn how RCA's regulatory compliance consultants approach the MDR submission process & clinical evidence requirements for CE Mark.
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Click to learn more about how a certified internal auditor can help life sciences companies during a supplier, regulatory and internal audit.
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Click now to Learn from RCA's regulatory compliance consultants about data & the amount of capa records needed to open an investigation.
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