Recipharm’s Post

Ensuring Quality in Pharmaceutical Supply Chains: Our Commitment to Excellence The purpose of quality assurance (QA) in public pharmaceutical supply systems is to make certain that each medicine reaching a patient is safe, effective, and of standard quality. At Jeyflex, we understand that the integrity of pharmaceutical products is paramount. Our QA services encompass a comprehensive approach, spanning the entire supply process from medicine selection to patient use. Our dedicated quality assurance specialists work tirelessly to ensure that every product meets and exceeds the respective regulator’s quality standards. Trust Jeyflex to deliver excellence in every step of the pharmaceutical supply chain, ensuring safety and efficacy for the end-user. #Pharmaceuticals #QualityAssurance #Healthcare #Jeyflex #PatientSafety #RegulatoryCompliance #PharmaExcellence

QUALITY:- Upholding Quality In the pharmaceutical industry, quality is paramount. Every step we take ensures that we are delivering safe, effective, and reliable medications to patients worldwide.I am proud to be part of a team that prioritizes excellence in every aspect of our work. Our mission is to continuously improve and innovate, ensuring that every product we produce meets the rigorous standards that our Patient's demand. Quality isn't just a benchmark; it's our promise to those who rely on us. Together, we are making a difference and setting new standards in pharmaceutical excellence. #PharmaceuticalQuality #ExcellenceInPharma #PatientSafety #ContinuousImprovement #InnovationInPharma #Quality #QualityControl

The solutions we provide here at eSA:   As long as we have been around, we have helped support the submission of New drug application eCTD packages. However, just 5 years ago we also began providing support for drug master file (DMF) eCTD packages as well. As of now, we support the submission of over 100 applications centered in Japan.   We have helped support a wide variety of DMFs, the main types have been Type II (Drug Substance), Type III (Packaging Material), and Type IV (Excipient). While it was expected that type III submissions would become mandatory in 2018, as the deadline approached, this never came to be and is still not mandatory to this day. https://lnkd.in/gxsyVNnv https://lnkd.in/gCxNfvMg   Regardless of region, leave all of your eCTD submission needs to eSA! #ectoderm #regulatoryaffairs #pharmaceutical #pmda #fda #edqm #ema #publishingservices #swissmedic #tga #healthcanada #incountrycaretaker #solutions #globalregulatory

#PatientEngagement Country Guidelines for #Canada are now available ⛳️ Discover the Guidelines for country codes of conduct that govern interactions between #Pharmaceuticals & #patient community. Explore now: https://lnkd.in/dSFR9vwn

📢 Attention pharmaceutical industry professionals! The World Health Organization (WHO) has released new guidelines for excipients used in pharmaceutical products. These guidelines include an appendix listing examples of high-risk excipients that are restricted due to their potential to cause cancer and other severe diseases. We are proud to say that our patented technology has allowed us to produce excipientless dosage forms since 2006, in line with these latest guidelines. Stay informed and ensure the safety of your pharmaceutical products by following the WHO's guidelines for excipients. Let's work together to prioritize the health and well-being of patients around the world. #pharmaceuticals #WHOguidelines #excipientsafety #patienthealth

Protecting Confidential Clinical Trial Data: A Global #Pharma Success Story When a global pharmaceutical leader needed to securely share sensitive clinical trial data with external research agencies and regulators like the FDA and EMA, they turned to Seclore. Discover how our solution transformed their data security while enabling seamless collaboration: https://lnkd.in/gpiW9YGY #ClinicalTrials #HealthTech #HealthIT #EMA #FDS #DataSecurity #Pharmaceutical #PharmaTech #HealthcareSecurity

I'm excited to share my latest blog post: [Understanding ICH and Its Role in Global Pharmaceutical Regulation](https://lnkd.in/dPX_yESG) In this post, I dive deep into the International Council for Harmonisation (ICH) and its critical impact on the global pharmaceutical landscape. Discover how ICH guidelines streamline drug development, ensure quality, and enhance patient safety worldwide. Key takeaways: 🔹 What ICH is and its mission 🔹 The significance of harmonized guidelines 🔹 How ICH influences regulatory processes globally Whether you're a regulatory professional, a pharmaceutical enthusiast, or just curious about the intricacies of drug regulation, this post is for you! Please read the full article here: [Understanding ICH and Its Role in Global Pharmaceutical Regulation](https://lnkd.in/dPX_yESG) Let's discuss how ICH shapes the future of pharma. Your thoughts and feedback are most welcome! 💬💡 #Pharmaceuticals #RegulatoryAffairs #ICH #DrugDevelopment #GlobalHealth #PatientSafety #PharmaRegulation

🚨MHRA Green Guide: A Game-Changer for UK Pharma Manufacturing The 2022 updates to the MHRA Green Guide have ushered in a new era for pharmaceutical manufacturing in the UK. As the regulatory landscape evolves, the emphasis is now on domestic production and stringent compliance to maintain the highest standards of safety and quality. With these guidelines, it's crucial for products intended for the UK market to be manufactured and stored under conditions that meet the strictest regulatory requirements. 🏢This is where Astoriom comes in: - Our cutting-edge ICH storage facilities ensure that your products are stored under optimal conditions, fully compliant with UK standards. - Expert management: Our team is well-versed in the latest regulatory requirements, dedicated to maintaining the integrity of your pharmaceutical products. - Strategically located in the UK: Our facilities are positioned to support efficient manufacturing and distribution processes, ensuring your products reach the market seamlessly. Let's work together to keep the UK at the forefront of pharmaceutical innovation and safety. 💪 #Pharmaceuticals #MHRA #ICHStorage #UKManufacturing #Astoriom #Compliance

To guarantee that #patients have access to safe, efficient, and high-quality generics, the FDA highlights how important it is to advance the development of complicated #genericdrugs. There is a drive for early interaction between generic #medicine makers and #regulatory agencies due to the recognition of the significant expenditure in #researchanddevelopment needed. The #FDA's #CDER Office of Generic Drugs and the European Medicines Agency have launched a voluntary pilot program, which is a noteworthy step in this direction. The objective of this program is to enable concurrent dialogues between applicants for generic drugs and various #regulatory bodies, with a particular focus on enhancing accessibility to complicated generics, which the #EMA also refers to as "#hybrid medicines." This initiative builds on the partnership that already exists through the Parallel Scientific Advice program, highlighting a mutual commitment to improving patient access to these essential medications. Connect, Repost & Follow for more info on the pharmaceutical industry 🌍 #pharma #pharmaceutical #pharmaindustry #europe #pharmaceuticalindustry #healthcare

👨🔬👩🔬 𝗜𝗻𝗱𝘂𝘀𝘁𝗿𝘆 𝗜𝗻𝘀𝗶𝗴𝗵𝘁: 𝗨𝗻𝗱𝗲𝗿𝘀𝘁𝗮𝗻𝗱𝗶𝗻𝗴 𝗡𝗶𝘁𝗿𝗼𝘀𝗮𝗺𝗶𝗻𝗲 𝗥𝗶𝘀𝗸 𝗶𝗻 𝗣𝗵𝗮𝗿𝗺𝗮𝗰𝗲𝘂𝘁𝗶𝗰𝗮𝗹𝘀 As regulatory bodies like the FDA and EMA tighten guidelines around nitrosamines, it’s crucial for pharmaceutical companies to stay ahead. Dive into our R&D pharmaceutical labs and explore how innovative detection techniques are reshaping safety standards, validating precise research methodologies to accurately detect both simple and complex nitrosamines in pharmaceutical products. 𝗦𝗼, 𝘄𝗵𝗮𝘁’𝘀 𝗻𝗲𝘄 𝗶𝗻 Mérieux NutriSciences - Italia? It has been fully validated a suitable high sensitivity method for 𝗡-𝗡𝗶𝘁𝗿𝗼𝘀𝗼 𝗕𝗲𝘁𝗮𝗵𝗶𝘀𝘁𝗶𝗻𝗲 𝗼𝗻 𝘁𝗮𝗯𝗹𝗲𝘁𝘀 through 𝗨𝗛𝗣𝗟𝗖-𝗠𝗦/𝗠𝗦 𝘄𝗶𝘁𝗵 𝗟𝗢𝗤 𝟭𝗽𝗽𝗯. ➡ 𝗡𝗲𝘄 𝘃𝗮𝗹𝗶𝗱𝗮𝘁𝗲𝗱 𝗺𝗲𝘁𝗵𝗼𝗱 𝗮𝘃𝗮𝗶𝗹𝗮𝗯𝗹𝗲! Do not hesitate to send me a message to ask your questions! #Mxns #Pharmaceuticals #Nitrosamines #DrugSafety