Verification vs. Validation – Product Process Software and QMS 2018

Verification vs. Validation – Product Process Software and QMS 2018
Event on 2018-01-22 09:00:00
Course "Verification vs. Validation – Product Process Software and QMS" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This course will review the company Master Validation Plan for major key inputs and CGMP deficiencies. It will address the FDA's newer and tougher regulatory stance. This course's aim is to prove "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts. It will teach participants to evaluate its elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management. This course will evaluate different field-tested, U.S. FDA-reviewed V&V protocols; how to employ equipment/process Requirements Specs / DQs, IQs, OQs, and PQs, or their equivalents per ASTM E2500, all against a background of limited company resources. It will review a matrix that simplifies "as-product", in-product", process and equipment, et al, software VT&V, to assure key FDA requirements are not overlooked. While considering the QMS and 21 CFR Part 11; this course will make practical application of these same in two hands-on sessions. Why you should attend: This session helps participants: Understand Verification and Validation, differences and how they work together;Discuss recent regulatory expectations;Know how to document a "risk-based" rationale, and use it in a resource-constrained environment;Determine key "milestones" and "tasks" in a project;Locate and document key subject "inputs";Compile "generic" Master and Individual Validation Plans;Learn the key element of a Product V&V File/Protocol;Understand how to develop Process and/or Production/Test Equipment V&V Files/Protocols;Get a grasp of basic Test Case construction;Understand sample sizes and their justification;Learn the key elements of Software V&V expected by the FDA and how to document;Deal with hardware and software vendors, sales and marketingConsider a field-tested software V&V documentation "model";See how to compile QMS Electronic Records and Electronic Signatures V&Vs to satisfy 21 CFR Part 11. Who will benefit: This workshop will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning and V&V activities / plan(s). This information addresses Medical Devices, Pharmaceutical, Diagnostic, and Biologics requirements and implementation. The employees who will benefit include: Senior and middle management and staffRegulatory AffairsQuality Assurance or Quality Control ProfessionalsQA/QCIT/ISR&DProduction ManagementManufacturing EngineersProcess EngineersSoftware EngineersProject ManagersHardware and software vendors, sales and marketingAny professional tasked with V&V responsibilities Agenda: Day 1 Schedule Lecture 1: Master Validation Planning and the Master Validation Plan(s) Lecture 2: Product, Process / Equipment Hardware V&V Lecture 3: Product / Device V&V Lecture 4: Software V&V Lecture 5: Quality Management System / 21 CFR Part 11 V&V Lecture 6: Summary of morning discussion Lecture 7: Group activity on the MVPs Lecture 8: Review of group activity and Q&A Day 2 Schedule Lecture 1: Software V&V documentation "model" Lecture 2: Software V&V protocols – "black box", "white box" Lecture 3: Electronic Records and Electronic Signatures (Part 11) Lecture 4: Summary of morning discussion Lecture 5: Group activity on 1) hardware / equipment, and 2) software V&V protocols Lecture 6: Review of group activity and Q&A Lecture 7: Course summary discussion Lecture 8: Summary of morning discussion Lecture 9: Group activity on the MVPs Lecture 10: Review of group activity and Q&A Speaker John E Lincoln Consultant, Medical device and Regulatory affairs, John E Lincoln is Principal of J. E. Lincoln and Associates LLC, a consulting company. John, a graduate of UCLA, is a medical device and Regulatory Affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management and U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and have been described in peer-reviewed technical articles and workshops worldwide. John has also managed pilot production, regulatory affairs, product development/design control, 510(k) submissions and risk management per ISO 14971 and implemented projects. With over 28 years of experience in the FDA-regulated medical products industry, he has worked from start-ups to Fortune 100 companies, including Abbott Laboratories, Hospira, and Tyco/Mallinckrodt. Location: St. George UT Date: January 22nd & 23rd, 2018 and Time: 9:00 AM to 6:00 PM Venue: Hilton Garden Inn St. George 1731 South Convention Center Drive, Saint George, Utah, 84790, USA Price: Price: ,295.00 (Seminar Fee for One Delegate) Register now and save 0. (Early Bird) Until January 01, Early Bird Price: ,295.00 From December 31 to January 20, Regular Price: ,495.00 Register for 5 attendees Price: ,885.00 ,475.00 You Save: ,590.00 (40%)* Register for 10 attendees Price: ,122.00 ,950.00 You Save: ,828.00 (45%)* Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry. As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants. For More Information- https://www.globalcompliancepanel.com/control/sponsorship Contact us today! NetZealous LLC DBA GlobalCompliancePanel john.robinson@globalcompliancepanel.com support@globalcompliancepanel.com Toll free: +1-800-447-9407 Phone: +1-510-584-9661 Website: http://www.globalcompliancepanel.com Registration Link – http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901450SEMINAR?ticketleap-January-2018-SEO Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/ Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/ Follow us on Twitter: https://twitter.com/GCPanel Seminar Fee for One Delegate – 95.00

at The Hilton Garden Inn
1731S.ConventionCenterDrive
Saint George, United States

Regulatory Requirements and Principles for Cleaning Validation 2017

Regulatory Requirements and Principles for Cleaning Validation 2017
Event on 2017-09-14 09:00:00
Course "Regulatory Requirements and Principles for Cleaning Validation" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

Overview:

This 2 day course will cover practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. This two day interactive course will cover fundamental principles of a cleaning validation program, exploring such concepts as the determination of residues to be targeted, selection of analytical and sampling methods, determination of appropriate limits in various pharmaceutical and biotechnology processes, and establishment of scientific rationales acceptable to regulatory inspectors.
The program will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, a "Cleaning Validation Master Plan" and the appropriate documentation for each study to be performed. In addition, requirements for maintenance of the validated status will be reviewed. Regulatory requirements and the latest industry practices will also be included in the discussion.

Why you should attend:

Attendance at 2 day seminar will be beneficial to personnel directly involved in the development of cleaning procedures, cleaning validation programs and plans. Additionally, those responsible for cleaning validation protocols and execution activities, including validation and laboratory personnel, as well as, beginning or seasoned operational personnel who will eventually participate in such efforts, will find this course particularly useful. This includes Analytical Method Development, Quality Control and Quality Assurance personnel.
Individuals in management who interact with the above or communicate with regulatory agency inspectors to rationalize or defend cleaning validation programs will also benefit from attending this course. There are no prerequisites for attending, but a basic knowledge of general science and equipment cleaning processes is helpful.

Areas Covered in the Session:

• Understand the importance and underlying principles of cleaning validation and the requirements to have adequate cleaning procedures for manufacturing equipment in contact with the product
• Understand the FDA perspectives on cleaning validation and areas of concern during regulatory inspections
• Be able to set up cleaning validation procedures, protocols and reports that meet current FDA, WHO, PIC/S and EU regulations
• Prepare and defend your own cleaning validation approach/program and avoid costly delays and/or rejections by regulatory agencies

Who Will Benefit:

Attendance at 2 day seminar will be beneficial to personnel directly involved in the development of cleaning procedures, cleaning validation programs and plans. Additionally, those responsible for cleaning validation protocols and execution activities, including validation and laboratory personnel, as well as, beginning or seasoned operational personnel who will eventually participate in such efforts, will find this course particularly useful. This includes Analytical Method Development, Quality Control and Quality Assurance personnel.
Individuals in management who interact with the above or communicate with regulatory agency inspectors to rationalize or defend cleaning validation programs will also benefit from attending this course. There are no prerequisites for attending, but a basic knowledge of general science and equipment cleaning processes is helpful.
• Senior Quality Managers
• Quality Professionals
• Production Supervisors
• Validation Engineers
• Process Owners
• Quality Engineers
• Quality Auditors

Agenda:

Day 1 Schedule

Lecture 1:
FDA Requirements and Industry Standard Practices
Lecture 2:
How to Develop/Review your Cleaning Procedures and the Adequate Selection of Cleaning Agents and Parameters
Lecture 3:
How to Develop a Cleaning Validation Policy/Program
Lecture 4:
How to Implement a Robust Cleaning Validation Plan

Day 2 Schedule

Lecture 1:
Laboratory Issues in Cleaning
Lecture 2:
Microbiological aspects of a cleaning validation program for manufacturing equipment
Lecture 3:
Keys to Cleaning Validation Maintenance – Remaining Compliant
Lecture 4:
Current FDA concerns about validation of cleaning processes

Speaker
Joy McElroy
Principle Consultant, Maynard Consulting Company

Upon earning a degree in Zoology at North Carolina State University, Joy made her debut in the pharmaceutical industry in 1992 at Pharmacia & Up John performing Environmental Monitoring and Sterility Testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their Quality Control Lab.
Now with 12 years experience as a consultant, and over 20 years total experience in the pharmaceutical and biotech industries, Joy has gained extensive knowledge of Quality Assurance, Process and Cleaning Validation, and Equipment Qualification. She has written and executed Equipment Qualification and Validation Protocols for numerous Companies such as Mallinckrodt, Wyeth Lederle, Merck, BioMerieux, Catalent, Phillips Medisize, Xcelience, and Novartis.
Joy specializes in Equipment Qualification, Cleaning Validation,Sterilization, Environmental Monitoring, and GMP Compliance Auditing

Location: San Diego, CA Date: September 14th & 15th, 2017 and Time: 9:00 AM to 6:00 PM
Venue: WILL BE ANNOUNCED SOON, San Diego, CA
Price:

Register now and save 0. (Early Bird)
Price: ,295.00 (Seminar Fee for One Delegate)
Until August 10, Early Bird Price: ,295.00 From August 11 to September 12, Regular Price: ,495.00
Register for 5 attendees Price: ,885.00 ,475.00 You Save: ,590.00 (40%)*

Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar

At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry.
As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.
For More Information- https://www.globalcompliancepanel.com/control/sponsorship

Contact us today!

NetZealous LLC DBA GlobalCompliancePanel
john.robinson@globalcompliancepanel.com
support@globalcompliancepanel.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com

Registration Link – http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901170SEMINAR?eventful-September-2017-SEO

Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/
Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/
Follow us on Twitter: https://twitter.com/GCPanel

at San Diego, California, United States
San Diego, California, United States
San Diego, United States

Phone Validation Service with 98% Accuracy Gets Rid of Bad Phone Data

Clearwater, FL (PRWEB) August 19, 2013

RealPhoneValidation is an essential new tool for companies that rely on accurate, up to date phone data. It works by combining state of the art telephony technology together with a seamless API and web interface to quickly verify phone connectivity, eliminating a serious choke point.

With the leads industry showing a quick decline in quality over the past few years, RealPhoneValidation made a move to start cleaning up the industry. Building on their parent company’s 25 years in telephony, they have developed a service that solves an industry wide problem: telephone disconnects.

For those in the leads business, this is an opportunity to push problems back to the affiliates who provide a significant portion of the bad data in the market, and to re-contact those customers who enter bad data to begin with. The service is available in real-time as well as for batch processing.

By providing a product that vastly outperforms the industry standard of 75 percent accuracy, RealPhoneValidation is hoping to truly eliminate a problem that has plagued the industry for years, and has become a big business as data validation has grown.

RealPhoneValidation serves clients from hundreds to millions of calls per month. The company automates large data handling, giving buyers and sellers a trusted third party for phone verification. Prices start as low as a few pennies per call. Its comparable to making a simple phone call, and eliminates the need for a live body to make calls. RealPhoneValidation is offering 1,000 free trial validations so prospective clients can see this essential tool in action.

To learn more visit RealPhoneValidation.com

About RealPhoneValidation:

Built for those in the contact industry, RealPhoneValidation is an API and batch processing service that is as simple as the name it really validates phones. To find out more, go to http://www.RealPhoneValidation.com. RealPhoneValidation is a service of TotalContactSolutions, Inc. dba VOISYS.







Startup-Académie 202 – Validation (31 mai-5 juillet, Montréal)

Startup-Académie 202 – Validation (31 mai-5 juillet, Montréal)
Event on 2013-05-31 21:00:00


Avez-vous une idée de startup technologique qui pourrait changer le monde?
Pouvez-vous bâtir une entreprise à succès autour de votre idée? 

Cette deuxième étape de la série Startup-Académie vous présentera des outils incontournables pour valider votre idée de startup – qui seront vos premiers clients, pourquoi achèteront-ils votre offre, et quelle est l'élément déclencheur pour que votre offre devienne virale.

Cet atelier avant-gardiste vous présentera des outils indispensables qui vont révolutionner vos résultats, incluant les concepts du « Lean Startup », le « Customer Discovery and Validation » et le « Validation Board ».

Vous apprendrez comment:

– Définir avec précision les caractéristiques et les qualités de votre utilisateur initial;
– Sonder vos clients potentiels pour découvrir le problème urgent qu'ils veulent voir résoudre et comment votre offre résoud leur situation;
– Déterminer l'élément décisionnel déclencheur pour que votre prospect saute sur votre offre;
– Choisir les outils pour trouver, garder et générer des clients;
– Monter un premier Produit Minimal Viable (MVP) pour évaluer comment vos premiers clients réagiront à votre offre;
– Tester les prix, tarifs, forfaits et autres formes de revenus, pour que votre startup démontre sa crédibilité en générant du revenu dès le jour 1;
– Identifier les éléments de risque de votre modèle d'affaires et les stratégies pour gérer ces risques.

À la fin de ce processus vous aurez tous les éléments pour évaluer la viabilité de votre startup, et les outils pour monter votre première offre et attirer vos premiers clients.  

Cet atelier est essentiel si vous désirez lever du capital soit par des anges investisseurs, le « love money », le « crowdfunding » ou même avec vos propore ressources. Vous ferez plus de 100 entrevues avec des clients, des partenaires et d'autres parties prenantes potentiels pour démontrer sans hésitation à vous et à vos investisseurs potentiels que votre projet a tout ce qu'il faut pour réussir.

Cet atelier de cinq semaines s'adresse à tout type de startup basé sur un avantage technologique innovateur, que vous soyez à l'étape de définition de votre idée, d'amorçage ou de recherche de financement:

– logiciel, web, applications mobiles, social;
– biotech (autre que pharma et thérapeutiques);
– technologies vertes ou du développement durable;
– technologies industrielles (électronique, optique, photonique, mécanique, énergie)
– produits pour le B2C (marché de masse) ou pour le B2B (entreprise à entreprise)

Votre investissement vous donne droit à:

– Trois jours (20 heures) de formation et de coaching en salle pour comprendre et appliquer des outils de pointe qui vous feront sauver du temps et de l'argent dans le lancement de votre startup;
– Cinq webinaires (10 heures) de formation et de coaching pour répondre aux questions et aux embuches que vous allez rencontrer lors de vos activités de validation;
– Accès au coaching (jusqu'à 5 heures par équipe en rencontre individuel, ainsi que accès illimité par courriel);
– Accès à un site privé plein de ressources;
– et d'autres avantages qui vous seront communiqués sous peu.

Des forfaits d'inscription sont disponibles pour les entrepreneurs individuels ainsi que les équipes (jusqu'à trois associés par équipe).

Le programme est limité à 7 (sept) projets (équipes ou promoteurs individuels), et sera livré en français (certains documents seront en anglais).

À propos de votre mentor-coach, Coach Davender Gupta, MSc

« Coach » Davender offre l'expérience de trois carrières aux startups ambitieux. Il fut d'abord un ingénieur de recherche et développement aérospatial dans l'Aviation royale canadienne pendant quinze ans, où il acquit une expérience unique en gestion de projets. En 1995, il démarre sa propre entreprise en imagerie numérique, pour ensuite participer dans le lancement d'un startup technologique en 1998-99. Cette aventure lui donne l'opportunité de devenir un coach professionnel d'entrepreneurship en 2000, accompagnant depuis ce temps des centaines d'entrepreneurs à travers le Canada, les États-Unis et l'Europe. Son plus récent projet est Startup-Académie, un accélérateur virtuel basé à Québec qui vise à développer les connaissances, les compétences et la confiance des entrepreneurs haute-performance. Davender est très actif dans l'écosystème des startup technologiques au Québec. Parmi ses plusieurs implications, il est le coach-en-chef du bootcamp FastTrac TechVenture Québec, il siège au comité aviseur de StartupCanada, et il est le Vice-président du CA du CLD de Québec.

Partenaires de l'activité:

 

  

 

 

 

 

 

Agenda:

Jour 1: Monter votre stratégie de validation (vendredi 31 mai, accueil 8h30, activité 9h-17h)
Jour 2: Déterminer l'élément déclencheur et votre MVP (vendredi  14 juin, accueil 8h30, activité 9h-17h)
Jour 3: Journée de présentation de vos résultats (vendredi 5 juillet, accuel 8h30, activité 9h-17h)

Webinaires de coaching – 
Mercredis soirs 19h-21h
5-12-19-16 juin et 3 juillet

Sessions de «bureau ouvert» (disponibilité de coaching individuel sur demande)

Accompagnement total: plus de 40 heures de contact  

Lieu:

Bureaux de Rho Canada Ventures
1800 McGill College Avenue, Suite 840, Montreal, Quebec H3A 3J6 

 

Pré-requis:

Pour être éligible à participer à ce programme, vous devez avoir en main un canevas de modèle d'affaires préliminaire (style Osterwalder ou Lean Canvas) et avooir complété au moins un des pré-requis suivants:

– Weekend Startup-Académie 101 (Définition), ou
– FastTrac TechVenture Québec, ou
– Startup-Weekend (Montréal, Québec ou ailleurs), ou
– le cours vidéo « How To Build A Startup » de Steve Blank (https://www.udacity.com/course/ep245)
– Lean Launchpad, NEXT, Lean Startup Machine, ou
– une formation sur le canevas de modèle d'affaires (validé avec une entrevue avec Coach Davender), ou
– une référence d'un programme d'accélération ou d'un investisseur, ou
– une entrevue avec Coach Davender.

Votre inscription à Startup-Académie 202 vous donne droit à participer, sans frais supplémentaire, au weekend Startup-Académie 101 (10-11-12 mai à Montréal ou 7-8-9 juin à Québec).

 

Investissement:

Équipe: 1999,00$ (plus frais Eventbrite et plus taxes) – Ce billet donne droit à jusqu'à trois partenaires d'un même projet de startup à participer au programme INCLUANT le weekend Startup-Académie 101

Individuel: 1499,00$ (plus frais Eventbrite et plus taxes) – Ce billet donne droit à un fondateur individuel à participer au programme INCLUANT le weekend Startup-Académie 101

Payable par PayPal ou carte de crédit (via PayPal)

À noter: une fois payée, votre inscription n'est pas remboursable, mais peut être transférée avec la permission de Coach Davender.

Un reçu conforme sera remis.

 

 

Inscription:

http://startup202-1304.eventbrite.com

 

Gestion Davender Gupta Inc. (Startup-Académie)
Complexe Jules-Dallaire, 2828 boul Laurier, Tour T1, suite 700
Québec (QC) G1V 0B9 

(Québec) 418-948-1553
(Montréal) 514-448-1894
coach@davender.com
www.startup-academie.com

NEQ: 1167122119
TPS: 825566805RT0001
TVQ: 1217890337TQ0001
Agrément de formateur Emploi-Québec:0055514

at Demers Beaulne
1800 avenue Mcgill college
Montreal, Canada

2-day In-person Seminar on “Design of Experiments and Statistical Process Control for Process Development and Validation” atPhiladelphia, PA

2-day In-person Seminar on “Design of Experiments and Statistical Process Control for Process Development and Validation” atPhiladelphia, PA
Event on 2013-05-23 09:00:00
Overview:
Examples from real processes and testing procedures will be used to present the student with examples that will be directly applicable to their work. This course will present the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes. A practical approach with case studies and examples will be used, with theoretical information introduced only when necessary to understand an experiment.

Course Outline:
Dietary Design of Experiments
Day 1 – Agenda
Lecture 1: Introduction
Lecture 2: One Level, One Factor Designs. Simple Comparisons.
Lecture 3: Two-Level Multi-factorial Design
Lecture 4: Extracting Information from the Experiment

Statistical Process Control
Day 2 – Agenda
Lecture 5: Shewhart Charts for Variable Data
Lecture 6: Shewhart Charts for Attribute Data Especially Counts.
Lecture 7: Considerations from Shewhart Charts
Lecture 8: Other Types of Charts Related to Shewhart Charts

Who Will Benefit:
Directors
Managers
Supervisors
Lead workers in Process Development
Manufacturing
Regulatory Affairs
Quality Assurance and Quality Control

ABPUT SPEAKER:
Dr. Steven S. Kuwahara Ph.D. is the founder and Principal of GXP BioTechnology LLC, a consulting firm that works in the areas covered by the GLP and GMP of drugs, biologics, and nutraceuticals.

DATE AND VENUE:
Location: Orange County CA | February 7th & 8th, 2013
Conference Timings: 9 am to 6 pm PST
WILL BE ANNOUNCED SOON

Price – ,295.00

Contact Information:
GlobalCompliancePanel
Event Coordinator
Toll free: 800-425-9409
Fax: 302-288-6884
http://www.globalcompliancepanel.com
Email: support@globalcompliancepanel.com

at Announcement Soon
Announcement Soon
South San Francisco, United States

Masy Systems Increases Validation Personnel in Pennsylvania and New Jersey

Philadelphia, PA (PRWEB) March 13, 2013

Masy Systems, Inc., a leader in validation services for over twenty-five years is pleased to announce the addition of new personnel operating out of a satellite location in Eastern Pennsylvania. Sylvan Poeckh joined the team in 2011 focusing on service efforts in the Pennsylvania-New Jersey area. The continued success in this area required additional staffing. Matt Groff joined the Validation team to provide a local validation service with highly qualified personnel.

Matt Groff joins Masy Systems from the Collegeville, PA area. Matt was awarded a full-tuition scholarship at the Webb Institute in Glen Cove, NY where he received his B.S. in Naval Architecture/Marine Engineering. While attending the Webb Institute Matt worked as a pipefitter on the USS Enterprise, spent two months at sea in the engine room of a Chemical tanker and worked in two design offices doing ship stability calculations and 3D modeling. Matt spent a summer semester at a Long Island company that manufactures pressure gauges, calibration hand pumps and loop calibrators for the gas industry. This experience, combined with his previous work and school experience spiked his interest in metrology and validation.

“Sylvan’s successful relationships with our customers, Matt’s strong technical skills, and Clive Smith as Masy’s Validation Product Manager allows us to properly address the needs of current and new customers in the local area. We have a very strong Validation Team able to service a large footprint with excellent, local representation” said Jason Daoust, Masy’s Business Development Manager.

Masy’s Validation division provides validation services for sterilizers, chambers and warehouses for numerous clients in North America. The company is NVLAP accredited to ISO 17025 for calibrations, and ISO 9001 certified. Masy provides validation and calibration services, equipment rentals, and GMP storage for the pharmaceutical and biotech industries.