Metamorph Global Inc

Name: Metamorph Global Inc
Address: 2350 Oak Park Road, Glendora, CA, 91741, US
Telephone: +16574528174

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United States
Glendora, CA
Metamorph Global Inc

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06/07/2024

Day 2 of the masterclass on GCP Quality Management Systems (QMS) from the FDA Perspective is happening right now with our expert trainer Lee Truax Bellows.

Stay tuned for more masterclasses in the pharmaceutical and biotech industry.

For any inquiries, contact us at [email protected] 📞 Contact us: +1 657 452 8174

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06/07/2024

🔬 Our highly anticipated masterclass on GCP Quality Management Systems is happening now! Join us for two days of expert insights into building a robust GCP QMS.

Stay tuned for industry-leading discussions on FDA regulations, risk management, root cause analysis, and more.

Don't miss out on future events shaping the pharmaceutical landscape. Follow us for updates!

🌐 Keep an eye out for future learning opportunities, networking sessions, and valuable industry insights!

06/07/2024

Join us for an exclusive masterclass led by Tara Scherder, a seasoned expert with over 20 years in the pharmaceutical industry.

As principal at SynoloStats, Tara combines statistical prowess with deep manufacturing and analytical sciences knowledge to optimize processes and manage risk effectively.

Don't miss this opportunity to learn from Tara's insights on Statistical Methods for Process Validation.

Limited seats available:
📧 Register at [email protected]
📞 Contact us: +1 657 452 8174

Registration Link - https://lnkd.in/dsbfekRG

06/07/2024

Final Call: Only 3 seats left!

Join us for a transformative workshop led by renowned expert Lee Truax Bellows.

Learn practical approaches and tools for implementing a Quality Management System in clinical trials, including essential concepts like GCP Risk Management and Root Cause Analysis. Reserve your spot now and take your clinical study conduct to the next level!

📩 Limited seats available! Reach out now at [email protected] or call us at +1 657 452 8174.

Don't miss out on this exclusive opportunity!

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06/07/2024

🔬 Our highly anticipated masterclass on analytical procedure validation is underway! Stay tuned for industry-leading insights from our experts.

Don't miss out on future events shaping the pharmaceutical landscape. Follow us for updates!

🌐 Keep an eye out for future learning opportunities, networking sessions, and valuable industry insights!

06/07/2024

Celebrating another milestone in our journey of empowering industries with knowledge! 🚀 Grateful for the steadfast support and collaboration of our valued partners.

Connect with us via email at [email protected] or give us a call at +1 657 452 8174.

Together, let's pioneer the future of education! 🌐

06/07/2024

Meet our esteemed trainer, Stephanie Pasas-Farmer, who will guide you through our upcoming masterclass on Balancing Innovation, Efficiency, and Safety with Regulations: Employing AI in the Pharmaceutical Industry.

Don't miss this opportunity to gain invaluable insights from an expert in the field.

📩 Limited seats available! Reach out now at [email protected] or call us at +1 657 452 8174.

Registration link - https://lnkd.in/gKeypyqF

06/07/2024

🔥 Don't miss out on our upcoming masterclasses in May 2024, led by industry experts in Pharma and Biotech!

🌟 Limited spot available, so secure yours now!

🔍 Stay ahead with exclusive online courses.

Registration closing soon! Reach out to us:
📧 [email protected]
📞 +1 657 452 8174

06/07/2024

Dive deep into the latest in Annex 1 GMP Compliance! Join us for a comprehensive masterclass exploring 15 Key Impact Topics over 3 dynamic days. From Protective Airflows to Rapid Micro Methods, and everything in between, gain invaluable insights to enhance your compliance strategy.

🔍 Day 1: Explore the nuances of Protective Airflows and Computational Fluid Dynamics, essential for airborne contamination control. Plus, delve into the intricacies of Open Barrier door setup and Contamination Control Risk Assessments. Join us for a deep dive into these crucial topics!

🔍 Day 2: From Rapid Micro Methods to Barrier Glove Management Strategies, Day 2 promises insights into cutting-edge technologies and compliance essentials. Don't miss discussions on Aseptic Containment Strategies and Data Integrity & Digitalization.

🔍 Day 3: Elevate your understanding of CCS preparation for Bioburden control processes and VHP cycle development. Plus, learn how to enhance Procedural Controls and Personnel Training for optimal compliance. Join us for a finale of high-impact insights!

📩 Limited seats available! Reach out now at [email protected] or call us at +1 657 452 8174.

Registration link- https://lnkd.in/d_7R4tgs

06/07/2024

Celebrating another successful stride in our journey of trust-building! 🌟 Grateful for the unwavering support and partnership of our esteemed clients.

Connect with us through email at [email protected] or ring us up at +1 657 452 8174.

Let's forge ahead together! 🔗

06/07/2024

Introducing our esteemed expert trainer, Dr. Lars J. Brandén, who will lead our upcoming masterclass on CMC for Cell and Gene Therapy, focusing on viral vectors.

With a wealth of experience in this field, Dr. Brandén is also conducting the masterclasses "Cell and Molecular Biology Mastery: From Basics to Breakthroughs" and "Mastering mRNA Therapeutics: From Fundamentals to Future Trends."

Join us in this interactive masterclass to gain insights from an unparalleled expert. Don't miss this opportunity to elevate your knowledge in pharmaceutical training.

📩 Limited seats available! Reach out now at [email protected] or call us at +1 657 452 8174.

Registration link - https://lnkd.in/g_8ruGVu

06/07/2024

🔬 Join our masterclass led by James, an industry luminary, as he navigates the intricacies of the revised EU GMP & PICS Annex 1 for sterile product manufacturing.

With a paradigm shift in GMP regulations, James will illuminate the holistic, risk-based approach essential for compliance.

🌟 This comprehensive training encompasses 15 high-impact topics, offering a proactive perspective on contamination control and sterility assurance. Engage in dynamic discussions to benchmark with peers and gain insights into meeting CGMP compliance standards.

Don't miss out on this transformative learning experience.

📩 Limited seats available! Reach out now at [email protected] or call us at +1 657 452 8174.

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06/07/2024

Join us now for the highly anticipated masterclass on Statistics for Quality Control and Quality Assurance, led by the esteemed Dr. Joachim Ermer.

We're thrilled to announce that the event is fully booked! A big thank you to all the participants for placing your trust in our educational programs.

🌐 Keep an eye out for future learning opportunities, networking sessions, and valuable industry insights!

06/07/2024

Each delivery reinforces trust! 🛠️ We're privileged by the confidence and collaboration of our esteemed clients from the recent Middle East auditing event.

Contact us via email at [email protected] or give us a call at +1 657 452 8174.

-Learning

06/07/2024

Our highly anticipated Masterclass for the Middle East market is happening now, with almost all seats fully booked!

A big thank you to our trainer, Phil Griffiths, for sharing expertise and insights.

🌐 Stay tuned for more learning opportunities, networking, and industry insights! 💼

06/07/2024

Meet our distinguished trainer, poised to lead the much-anticipated Advanced Process Validation masterclass on April 18th-19th!
With a wealth of experience in the pharmaceutical industry, he brings unparalleled expertise to empower professionals like you.

Elevate your skills and gain invaluable insights from a true industry expert. Don't miss out!

📩 Limited seats available! Reach out now at [email protected] or call us at +1 657 452 8174.

Registration Link - https://lnkd.in/gB7QC8yc

06/07/2024

🌟 Unlock Your Potential in April Masterclasses! 🌟

🔍 Explore Advanced Process Validation Strategies with Dr. Felix Tobias Kern. Gain insights into regulatory essentials, batch optimization, and seamless integration with Qualification Activities.

📊 Master Statistics for Quality Control and Assurance Practice (3rd Edition) with Dr. Joachim Ermer. Dive deep into statistical parameters crucial for Quality-by-Design, performance analysis, and routine control.

🔬 Delve into Final ICH Q2(R2) – Validation of Analytical Procedures (2nd Edition) with Dr. Joachim Ermer. Understand the evolution of analytical procedure validation, from traditional principles to modern Quality-by-Design approaches.

📩 Limited seats available! Reach out now at [email protected] or call us at +1 657 452 8174.

Don't miss out on this exclusive opportunity!

06/07/2024

Celebrating the bonds forged through exceptional service! 🌟 Grateful for the opportunity to work hand-in-hand with our esteemed client.

06/07/2024

🔍 Elevate Your Audit Expertise with Advanced Techniques for Major Projects!

📚 Day 1: Master the Art of Audit Involvement from Proposal to Review.

Discover how internal audit involvement throughout the project lifecycle maximizes success in delivering projects on time, within budget, and meeting stakeholder needs. Learn to promote audit benefits and apply risk-based approaches for effective project audits.

🔬 Day 2: Auditing Major Projects with Confidence & Identifying Warning Signs.

Gain confidence in auditing major projects and identifying early warning signs for proactive intervention. Implement proven techniques to ensure projects meet objectives and control risks effectively, even under pressure.

📧 For a detailed agenda, contact us at [email protected] or 📞 +1 657 452 8174.

Don't miss this opportunity to enhance your audit skills and contribute to project success!

06/07/2024

🔍 Explore Mastery in Clinical Trial Quality Management!

📚 Day 1: Unveil the Fundamentals of Quality System Approach in Clinical Studies.

Discover the pivotal role of Quality Management Systems (QMS) in clinical trial design, development, and ex*****on. Gain practical insights into risk management strategies essential for regulatory compliance.

🔬 Day 2: Navigating GCP Risk Management & Root Cause Analysis.
Dive deep into Good Clinical Practice (GCP) principles, mastering risk management techniques and Root Cause Analysis (RCA). Learn effective Corrective and Preventive Actions (CAPA) to ensure study integrity.

📧 For a detailed agenda, reach out to us at [email protected] or 📞 +1 657 452 8174.

Don't miss this opportunity to elevate your understanding of pharmaceutical regulatory excellence!

06/06/2024

🔍 Dive into Regulatory Excellence in Pharmaceutical Manufacturing!

📚 Day 1: Unveiling the Essentials of MAH Responsibilities & Regulatory Compliance.

Explore the intricacies of MAH obligations as outlined in the EMA "Reflection Paper" and integrated into EU GMP Guide Part III.

Understand the crucial role of regulatory compliance throughout the product life cycle, from submission to post-approval activities.

🔬 Day 2: Navigating the Terrain of Development, Manufacturing, and Control Strategies.

Delve into the nuances of development, manufacturing, and control strategies ensuring conformity with regulatory standards. Gain insights into stability monitoring, verification activities, and the holistic approach to pharmaceutical life cycle management.

📧 For a detailed agenda, reach out to us at [email protected] or 📞 +1 657 452 8174. Don't miss this opportunity to elevate your understanding of pharmaceutical regulatory excellence!

06/06/2024

🔍 Exciting News in Pharmaceutical Quality Control!

📊 Learn about the latest updates in analytical procedure validation from the revised Q2 guideline to Q14 "Analytical Procedure Development".

Dive into the changes, new recommendations, and critical discussions on addressing gaps and uncertainties.

Join us to explore the evolving landscape of Quality-by-Design principles and holistic life-cycle management in pharmaceuticals.

Don't miss out on mastering confidence intervals and gaining insights from practical examples.

📧 For detailed agenda, email us at [email protected] or 📞 +1 657 452 8174. Don't miss this opportunity!

06/06/2024

🚀 Dive deep into Process Validations in our upcoming masterclass! Learn about regulatory foundations, optimizing strategies, batch reduction techniques, batch scaling, combining validations with qualification activities, and effective documentation.

Don't miss out! 📧 For detailed agenda, email us at [email protected] or 📞 +1 657 452 8174.

Secure your spot now!

06/06/2024

Big thanks to our esteemed trainer and all the dedicated participants who engaged in our Final ICH Q2(R2) – Validation of Analytical event.

🌟 Stay connected for further enriching learning experiences, valuable networking opportunities, and profound industry insights! 💼

06/06/2024

🌟 Our eagerly awaited masterclass, "Exploring 15 Key Topics with High Impact Post-2023 - Annex 1 GMP Compliance," is currently underway with participants from all corners of the world, and it's completely packed! 🚀

🌐 Stay tuned for more learning opportunities, networking, and industry insights! 💼

06/06/2024

Unlock the secrets to Annex 1 compliance and revolutionize your approach to sterile product manufacturing. 🛡️

🎉 Our highly anticipated event, "Final ICH Q2(R2) – Validation of Analytical Procedures" by Dr. Joachim Ermer, is happening RIGHT NOW and it's fully booked!

🌟 Stay tuned for invaluable insights into pharmaceutical analytics.

06/06/2024

Each delivery solidifies trust! 🛠️ Honored by the trust and collaboration of our valued client.

06/06/2024

📢 Join us for an insightful three-day event with Tara Scherder, an industry expert with over 20 years of experience in the pharmaceutical industry. Enhance your knowledge on Lifecycle Process Validation, statistical methods, and risk management.

🗓️ The event is just a few days away! Book your registration now. 📩 Limited seats available! Reach out at [email protected] or call us at +1 657 452 8174.

Agenda Highlights:

Day 1:
🔹 Lifecycle process validation and design
🔹 Modelling populations to assure quality
🔹 Process performance data and sampling plans

Day 2:
🔹 Evaluating PPQ data
🔹 Variability and stability testing
🔹 Equivalence vs difference testing

Day 3:
🔹 Statistical methods for manufacturing
🔹 CPV program design and SPC
🔹 Data analysis best practices

Registration Link - https://lnkd.in/dsbfekRG

04/23/2024

📧 Register at [email protected]
📞 Contact us: +1 657 452 8174

Registration Link - https://lnkd.in/dsbfekRG

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Address

2350 Oak Park Road
Glendora, CA
91741

Telephone

+16574528174

Website

https://metamorphglobal.io/

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📢 Join us for an insightful three-day event with Tara Scherder, an industry expert with over 20 years of experience in the pharmaceutical industry. Enhance your knowledge on Lifecycle Process Validation, statistical methods, and risk management. 🗓️ The event is just a few days away! Book your registration now. 📩 Limited seats available! Reach out at [email protected] or call us at +1 657 452 8174. Agenda Highlights: Day 1: 🔹 Lifecycle process validation and design 🔹 Modelling populations to assure quality 🔹 Process performance data and sampling plans Day 2: 🔹 Evaluating PPQ data 🔹 Variability and stability testing 🔹 Equivalence vs difference testing Day 3: 🔹 Statistical methods for manufacturing 🔹 CPV program design and SPC 🔹 Data analysis best practices Registration Link - https://lnkd.in/dsbfekRG #PharmaIndustry #ProcessValidation #StatisticalMethods #Compliance #QualityAssurance #Pharma #LifecycleValidation #ProcessValidation #StatisticalMethods #RiskManagement #QualityAssurance #PPQ #SPC #DataAnalysis #CPV #PharmaceuticalIndustry #MetamorphGlobal #IndustryEvent #StatisticsInPharma

Click on the link below to reserve your spot now. https://metamorphglobal.io/.../statistics-for-quality.../ or Send an email to [email protected] #MetamorphGlobal #QualityControl #QualityAssurance #Statistics #PracticalLearning #Pharmaceutical #MasterClass

Unlock the secrets of successful analytical method transfer in the pharmaceutical industry with our online masterclass led by renowned expert, Dr. Joachim Ermer. Gain valuable insights and practical skills to optimize your method transfer processes, improve efficiency and ensure regulatory compliance. Join us for this comprehensive and interactive learning experience, designed for professionals in the pharmaceutical industry. By attending this masterclass, you will gain valuable insights and practical skills that will help you understand the latest regulatory guidelines and requirements required to implement best practices for method transfer. Don't miss out on this opportunity to learn from the best! Register now through the link in the first comment. #MetamorphGlobal #AnalyticalMethodTransfer #AnalyticalMethod #Pharma #PharmaceuticalIndustry #MasterClass #OnlineMasterClass

Are you a pharmaceutical professional looking to stay ahead in the industry? Join our #masterclass on #toxicology , #PDEValues, #cleaningvalidation , and #CrossContaminationRiskAssessment. Learn the best practices for managing and reducing cross-contamination risk in shared manufacturing facilities, as per PIC/S requirements. Get hands-on experience with risk management, PDE values, cleaning validation, and comprehensive risk assessment. Don't miss this opportunity to enhance your skills with the experts at #MetamorphGlobal Click on the link below to register now and reserve your spot! https://lnkd.in/gmtuwRNn or send an email to [email protected] #pharmaceuticalmanufacturing #riskmanagement #professionaldevelopment #pharmaceutical #manufacturing #quality #qualityassurance #qualitycontrol #onlinecourses #onlinemasterclass