Il prossimo 21-22 novembre avrà luogo un training workshop in lingua italiana promosso da Stilmas e DOC Validation dal titolo “Pharmaceutical Water & Steam Systems: Current International Industry Practices, Technological Trends and Regulatory News”.
Che argomenti verranno trattati?
Il seminario tratterà in generale di acqua e vapore per uso farmaceutico, con una panoramica completa in base alle direttive europee (EDQM/EMA), statunitensi (FDA/USP) e cGMP internazionali (Anvisa, WHO, PIC/S, etc.) supportata dall’esperienza globale di Stilmas e DOC relativa all’ispezione degli impianti.
Gli argomenti trattati nell’ambito delle clean utilities saranno: requisiti normativi, attuali criteri di design come da GEP e nuove tendenze tecnologiche, life-cycle della validazione e manutenzione, monitoraggio e controllo dei sistemi.
Quanto sono attuali queste tematiche?
Il materiale del seminario è aggiornato ai Regulatory Requirements del 2019, in particolar modo a causa della nuova monografia EP per Acqua per Iniettabili rilasciata ad aprile 2017 e alla bozza di revisione dell’EU GMP Annex 1 (dicembre 2017).
A chi è indirizzato questo seminario?
Il workshop è indirizzato ai professionisti e manager delle Industrie Farmaceutiche coinvolti nelle applicazioni dei sistemi di produzione di acqua e vapore ad uso farmaceutico (sistemi di Qualità QA e QC, Regolamentazione e Validazione, Ingegneria, Manutenzione e Produzione (API e sistemi di dosaggio).
Per ulteriori informazioni scrivere a: email@example.com
Stilmas at the cutting edge of digital innovation!
Our General Manager, Eng. Roberto Montaruli, will be a speaker during the round table at the XIV ASAP SERVICE MANAGEMENT FORUM 2017 that will be held in Sesto San Giovanni (Milan) – 7,8 November 2017.
The event will be focused on the necessary skills to satisfy the customer needs through the use of digital technologies. Indeed, new technologies are becoming more and more an incredible strength point for new business models. At the other side of the coin, these new technologies are generating a lack of proper competencies. So, the event will be an open discussion on how to reduce the gap between competencies and technologies evolution.
Stay tuned and visit the website for further information and registration.
“New EP Monograph 2017 for WFI Production by Membrane Processes: Regulatory & Technological Challenges for Industry”,
Группа компаний MASCO рада пригласить Вас на семинар по теме «Новая монография европейской фармакопеи по производству ВДИ с помощью мембранных процессов: нормативы, технологические аспекты, анализ рисков», который пройдет 21 ноября c 13:30 до 15:30 в рамках выставки Фармтех 2017 (МВЦ «Крокус Экспо», Павильон № 2, зал 8, Зона презентации В531).
Семинар проведет ведущий специалист по валидации компании DOC (группа компаний MASCO) г-н Паоло Курто.
После семинара мы приглашаем Вас отметить юбилей группы компаний MASCO на нашем стенде В219, где пройдет фуршет с дегустацией напитков.
Пожалуйста, подтвердите Ваше участие на адрес firstname.lastname@example.org. Промокод для предварительной бесплатной электронной регистрации на выставку: pha17eDHAR
Если у Вас возникли дополнительные вопросы, свяжитесь с нами.
С наилучшими пожеланиями,
Группа компаний MASCO
Stilmas S.p.A. Olsa S.p.A. DOC s.r.l.
Dear ladies and gentlemen!
The MASCO Group of companies is pleased to invite you to a seminar “New EP Monograph 2017 for WFI Production by Membrane Processes: Regulatory & Technological Challenges for Industry“, which will take place on November 21st from 13:30 to 15:30 at the Pharmtech 2017 (Crocus Expo IEC, Pavilion No. 2, Hall 8, Presentation Zone B531).
The seminar will be conducted by the leading expert of DOC Validation company (MASCO GROUP) Mr. Paolo Curto.
After the seminar we invite you to celebrate anniversary of the MASCO group at our stand B219, where a fourchette with drinks will take place.
Please confirm your participation at email@example.com. You can use our promo-code pha17eDHAR for free online registration to the exhibition.
If you have any additional questions, please contact us.
Stilmas S.p.A. Olsa S.p.A. DOC s.r.l.
Stilmas experts will contribute to the training seminar on NEW EU WFI MONOGRAPH which will be held on May 25th in Dublin.
How will this affect us all? Is the new WFI Monograph a game changer – an opportunity, or further risk? Hear an expert supplier’s point of view…
Our main speaker:
Mr. Paolo Curtó, graduated in 1984 with Master of Science & PhD in Chemical Engineering at Padua University (Italy). He has worked at DOC since 1997 as Managing Director. In the past he worked in well-known companies like Fidia S.p.a, Foster & Wheeler Group, Enichem S.p.a. He is steering committee member of Parenteral Drug Association (PDA Italy Chapter), an active member of ISPE and international Federation Pharmaceutical (FIP) and qualified trainer for many Regulatory Agencies throughout the world (Brazil, India, China, Italy, Greece etc.)
How to register: Please Contact Alf Gregg at: firstname.lastname@example.org
Mr. Paolo Leani, STILMAS Technical Director, will deliver two speeches during the upcoming two days APIC Annual Conference:
– Proper approach to Control and Monitoring: a deeper analysis of WFI System.
– “Thermocompression: Strengths – Weaknesses – Opportunities – Trends”
About APIC Annual Conference:
The Arab Pharmaceutical Industry congress (APIC) was designed to provide an innovative and comprehensive overview of the latest research developments in pharmaceutical machinery. Our events offer a platform for professionals to share knowledge, network and discuss trend in the pharmaceutical industry. Register now to join us in a day of knowledge sharing, networking and to get a chance to meet and get to know the services of pioneers in the filed.
Stilmas is delighted to be invited, as speaker, at the 3rd INTERNATIONAL CONGRESS ON RESEARCH, DEVELOPMENT AND TECHNOLOGICAL INNOVATION IN THE BIOPHARMACEUTICAL INDUSTRY that is held in the INTERNATIONAL CONVENTION CENTRE, HAVANA, CUBA.
The organizers, the Cuban Biotechnological and Pharmaceutical Industries, BioCubaFarma, and the Center for Pharmaceutical Research and Development (CIDEM) have created the opportunity for many specialists to meet and to share their experience and discuss the latest trends and technology news.
Once again, Stilmas is glad to contribute to the innovation of Biopharma industry in Cuba.
Masco Group is pleased to invite you to our Seminar, organized in collaboration with Melapack Kft. Process division dedicated to the Pharmaceutical and Cosmetic Industries.
Through the several lectures presented, it will be provided an update about the latest regulatory requirements and an anticipation about the ones that will become effective starting from 2017.
Moreover the latest technological trends related to the manufacturing of pharmaceutical and cosmetic finished products like sterile solutions, suspension and ointments will be shown through specific case studies coming from our experience.
The last part of the Seminar will be dedicated to the Quality matter and it will cover the qualification and validation aspects of material, equipment and containers in contact with the pharmaceutical drug formulation.
Entry is free, however places are limited, please register in advance to confirm your attendance.
For any additional information regarding the participation please fill the form below
“EU GMP NEW APPROACH: Commissioning and Qualification”
Masco is organizing a 2-day-Validation seminar, which will be held in St. Petersburg, 3 – 4 October 2016.
The topic of the event is the following: “EU GMP NEW APPROACH: Commissioning and Qualification”.
The seminar is focused on technical and regulatory aspects of validation of a pharmaceutical facility as per the latest EU GMP Annex 15 as well as NEW EP Monograph.
On October 4 a visit of “Polysan” factory (http://eng.polysan.ru/) is organized for all participants.
Fill the form below for any additional information regarding the participation.
The 2016 Stilmas’ training and seminar program is going ahead…
The next step will be in Spain, where Stilmas, in collaboration with its sister validation company DOC and its historical Spanish partner IMCO, will present on 28 and 30 of June a seminar session focused on the topic of the pharmaceutical water treatment with the latest regulatory news.
Do not hesitate to contact us filling the form below or writing to email@example.com directly in order to take part at this event.
Here below the detailed program:
Topic : Pharmaceutical Water & Steam Systems: Regulatory, GEPs, Validation and Operational Aspects as per International GMP Expectations
- 9.00 – 9.15 : Welcome
- 9.15 – 10.15 : Latest Regulatory Requirements and Good Engineering Practices (G.E.P.) – By Mr. Curtò, Managing Director DOC
- 10.15 – 11.15 : Current Industry Practices and Technological Trends – By Mr. Incardona, Sales Manager Stilmas
- 11.15 – 11.45 : Coffee Break & Networking
- 11.45 – 12.45 : Validation Life-Cycle of a New Systems as per latest EU GMP Annex 15 – Mr. Curtò, Managing Director DOC
- 12.45 – 13.45 : Operational and Maintenance Aspects – By Mr. Incardona, Sales Manager Stilmas
- 13.45 – 15.15 : Cocktail –Lunch
An excellent opportunity to meet and to share the Stilmas’ know-how came forth in Teheran last December.
Traditionally, each year Stilmas organizes various symposiums, seminars and workshops all over the world with the scope to discuss with professionals of pharma and biotech industry the latest technical news, analyzing every single detail of the clean utilities’ manufacturing chain.
The meeting in Teheran, organized by our historical local partner KOA, has seen the participation of 16 Iranian Pharmaceutical companies each one represented by more than one specialist from different departments.
Mr. Pirola, Stilmas sales and country manager, shared with customers the technical news related to the Pure Water Systems as well as benefits of different technical solutions Stilmas’ systems can offer.
The symposium was scheduled in three separate sessions, as follow:
|First Session||09:30 – 11:00|
|Break||11:00 – 11:30|
|Second session||11.30 – 12:30|
|Lunch||12:30 – 13:30|
13:30 – 15:00
In the first session Mr. Pirola explained topics such as: Pre- treatment system, Reverse Osmosis system for production of Purified Water and Thermocompressor for producing hot/cold Water for Injection and focusing that nowadays, this system has the possibility for production of Purified Water as well.
The second session was focused on Multiple Effect plants and Pure Steam generation systems.
In the last section, the distribution of Purified Water, Pure Steam and Water for Injection has been analyzed sharing all the experience that Stilmas has collected in its History regarding this technical and controversial topic.