Pharmaceutical Events -18-19 October 2010, Amman, Jordan:: 21-22 October 2010, Istanbul, Turkey

Upcoming events in the Pharmaceutical Industry

Event Name: Technology Transfer Of Pharmaceuticals
Event Date: 18-19 October 2010, Amman, Jordan:: 21-22 October 2010, Istanbul, Turkey
Event Place: Jordan , Turkey
Workshop Objectives: • Revisit the essential terminology and key principles related to Pharmaceutical technology transfer.

• Current trends in the pharmaceutical industry which have made successful technology transfer more critical than ever.
• Understand the principles and practice of Pharmaceutical technology transfer.
• Understand the practical issues involved with Pharmaceutical technology transfer and most common mistakes made during technology transfer.
• Interact with attendees who wish to have more clarity on the basics of Pharmaceutical technology transfer.

Who Should Attend:
This workshop is a must attend for professionals from the following Streams in pharma and biotech companies::

	Technology Transfer
	Technical Operations
	Senior Management
	Research & Development

	Manufacturing
	Analytical Research
	Quality Assurance
	Quality Control

Organizers: Prescription Pharma Support Pvt. Ltd.
Contact Person: Marcellina Lobo

Tel: + 91 22 3201 0513

Email ID: pps.pharmasupport@gmail.com, prescriptionpharmaevents@gmail.com

Registration Fee:
Per person : Rs. 14,500/- + Service Tax @ 10.3 % as levied by Govt. of India
Group Discount - for a group of 4 persons or more from the same organization
Per Person Rs. 13,100/- + Service Tax @ 10.3 % as levied by Govt. of India.

Make DD/Cheque payable at Mumbai in favour of "Prescription Pharma Support Pvt. Ltd. ” and courier to: PPS House, Plot No.6, RSC 12/21, Sector No.2, Charkop, Kandivali (West), Mumbai-400067.

Pharmaceutical Events -Ahmedabad-Hyderabad-17-18 August 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry

Event Name: Isolators, Barrier & Containment Technology in the Pharma Life Sciences
Event Date: 17-18 August 2010(Ahmedabad), 20-21 August 2010(Hyderabad)
Event Place: Ahmedabad,Hyderabad
Workshop Objectives: This workshop is suitable for the following personnel from pharma and biotech companies, responsible for activities involving

pharmaceutical water systems.

• Revisit the essential terminology and key principles related to sterile & aseptic processing

• Get recent updates on regulatory position on isolators, from EU, PIC/S, US FDA, as well as ISPE & PHSS initiatives for RABS.

• Understand the principles and practice of bio-decontamination of isolators & gassable RABS

• Explore the choice – Isolator, RABS, or Cleanrooms – using case studies and industry examples

• Understand the practical issues involved with isolation technologies, and how to avoid and solve them.

• Hear the speakers present GMP considerations for handling potent & sensitizing compounds, including segregation & separation

• Learn directly from the experience of the persons using isolation technology for the past few years in a leading Indian company

• Interact with attendees who wish to have more clarity on the basics of isolation technologies, before they plan to implement it within their organisations.

Who Should Attend: if you are a pharmaceutical professional or consultant in the foll. fields involved with sterile operations or with isolators.

•Manufacturing Operations

•Validation

•Quality Assurance

•Middle and Senior Management

•Engineering and Projects

•Regulatory Affairs

•Research & Development

Organizers: Prescription Pharma Support Pvt. Ltd.
Contact Person: Ms. Judith Nathan OR Marcellina Lobo

Tel: + 91 22 3201 0513 / 2967 8560-61 (extn 250)

Mobile No: +91 93240 52308

Fax: +91 22 2967 8565

Email ID: pps.pharmasupport@gmail.com, prescriptionpharmaevents@gmail.com

Registration Fee:
Per person : Rs. 14,500/- + Service Tax @ 10.3 % as levied by Govt. of India
Group Discount - for a group of 4 persons or more from the same organization
Per Person Rs. 13,100/- + Service Tax @ 10.3 % as levied by Govt. of India.

Make DD/Cheque payable at Mumbai in favour of "Prescription Pharma Support Pvt. Ltd. ” and courier to: PPS House, Plot No.6, RSC 12/21, Sector No.2, Charkop, Kandivali (West), Mumbai-400067.

Pharmaceutical Events-Jakarta -Indonesia-29 -30 July 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry

Event Name: Project Management and Change Control:Get it Right The First Time
Event Date: 29-30 July 2010
Event Place: Harris Hotel Tebet, Jakarta
Workshop Objectives:
•Understand the European and US GMP requirements and guidance related to project and change management

•Familiarise yourself with the project planning and the application of risk management tools

•Obtain tools for scheduling qualification, validation, training and SOP writing and learning activities and to allow for effective risk communication and thereby mitigation

•Prepare lean documentation that demonstrates the successful implementation of the project plan in accordance with the design specifications


Who Should Attend: Professionals in pharmaceutical, Biopharmaceutical and API manufacturing Facilities involved in:

•New projects

•Design & validation or facilities & equipment

•Process & product development

•Change management

•Audit of change control activities

•Validation and qualification

•Activities related to change control

•Quality Assurance

•Manufacturing Operations

•Regulatory Affairs personnel

•Personnel involved in licensing applications to the regulatory authorities

Organizers: Prescription Pharma Support Pvt. Ltd.
Contact Person: Mr. Rony Rianto on + 62 81808610171 or rianto@inovamitra.com
Mr. Rizwan Rustam on + 62 2198949630 or rizwan.rustam@inovamitra.com

Registration Fee: Per Person USD 200.00

Payment should be made by cheque to the foll. details:

Account Name : PT. INOVA MITRA

Account No. : 129 000 4867 111

Bank : Mandiri, Jakarta - Indonesia.

Pharmaceutical Events -Singapore-26 -27 July 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry

Event Name: Managing Pharmaceutical Water Systems
Event Date: 26-27 July 2010
Event Place: Holiday Inn Atrium, Singapore
Workshop Objectives: The objective of this workshop is to bring participants the regulations and most recent regulatory guidelines concerning pharmaceutical water systems as well as practical elements regarding how to implement the guidelines.
The program will address the purification, storage and distribution of water used for pharmaceutical manufacturing. Sessions will describe the latest technologies and practices available for the purification of water as well as system design, considering economic, chemical and microbiological requirements for the system.

Who Should Attend: This workshop is suitable for the following personnel from pharma and biotech companies, responsible for activities involving pharmaceutical water systems.
• Water Systems Design
• Ongoing Maintenance
• Laboratory Testing
• Production
• Quality Assurance
• Validation and Qualification
• Operation And Monitoring
• Regulatory Affairs
• Projects and Engineering

Organizers: Prescription Pharma Support Pvt. Ltd.
Contact Person: Ms. Preetha

Phone/Email: (+65) 6562 6708 OR (+65) 9140 7354 , ppsworkshops@gmail.com
Registration Fee: Per Person: SGD 1500,
Group Discount: Per Person : SGD 1350*
* For 3 persons or more from the same company.
Early Bird Discount: Per Person: SGD 1250**
** If the confirmation and payment is received before 15th July 2010.

Payment should be made to: DBS Bank Ltd., Singapore. DBSSSGSG.
For credit to: 033-901438-4, HDFC Bank Ltd.,Mumbai. HDFCINBB
For further credit to: HDFC Bank Ltd.,Mindspace Branch, Malad West, Mumbai.
Ultimate beneficiary: Prescription Pharma Support Pvt. Ltd. Account No. 04112320000637
Please Note: Wire Transfer (bank-to-bank) charges must be borne by the sender.
Confirmation will be sent on email on reciept of the Registration form and payment.

Pharmaceutical Events -28-29-June 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry

Event Details: Preparing And Facing Regulatory Audits: A Practical Approach
Speaker: Maija Hietava-Lorenzi
Date & Venue:17-18 June 2010, Istanbul, Turkey

Details: The QC laboratory is essentially responsible for more than 50% of product safety and efficacy if you consider that they test raw materials, in-process materials and finished product, as well as perform stability testing, tests for process validation, cleaning validation, equipment validation and other validations and they also develop and validate analytical methods. Any company therefore relies heavily on the integrity of the data provided by its QC laboratory. This course will provide a detailed review of current regulatory requirements relating to GMPs in the laboratory as well as current industry practices.

The Workshop Leader for this event is Maija Hietava-Lorenzi, who has tremendous experience and expertise in this area. Maija used to be registered in EMEA as an EMEA Expert. She has represented the EU Commission, PQ program of WHO Geneva, and National Agency for Medicines Finland, as a Senior Pharmaceutical Inspector. She has worked in WHO PQ programme and performed GMP and GCP inspections worldwide. She has a wide experience in different positions in pharma industry and latest in biotech industry as VP - QA and Analytical Development, FIT Biotech and QP in Ark Therapeutics Oy in Finland.

for more info visit:www.pharmasupport.in

Get registration for this event visit: pharma-event-registration

Pharmaceutical Events -21-25-June 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry.

Event Details: Preparing and facing Regulatory Audits: A Practical Approach
Speaker: Maija Hietava-Lorenzi
Date & Venue:21-22 June 2010, Mumbai, 24-25 June 2010, Hyderabad

Details: The Workshop Leader for this event is Maija Hietava-Lorenzi, who has tremendous experience and expertise in this area. Maija used to be registered in EMEA as an EMEA Expert, when working in the Finnish Medicines Agency as a Senior Inspector. She has represented the EU Commission, PQ program of WHO Geneva, and National Agency for Medicines Finland, as a Senior Pharmaceutical Inspector. She has also been an Instructor in the Regulatory Compliance School, Ministry of Health in Italy, and has conducted various inspections on behalf of the EU Commission EMEA, NAM, PIC/S, and also AFSSAPS France with French Inspectors through an exchange program of European Commission. She has worked in WHO PQ programme and performed GMP and GCP inspections worldwide. In Africa she has worked in different programs for WHO, WHO PQ and AEDES. She has a wide experience in different positions in pharma industry and latest in biotech industry as VP - QA and Analytical Development, FIT Biotech and QP in Ark Therapeutics Oy in Finland.

for more info visit: www.pharmasupport.in
Get registration for this event visit: pharma-event-registration

Pharmaceutical Events -17-18-June 2010 - PharmaSupport.in

Upcoming events in the Pharmaceutical Industry.

Event Details: Preparing And Facing Regulatory Audits: A Practical Approach
Speaker: Maija Hietava-Lorenzi
Date & Venue:17-18 June 2010, Istanbul, Turkey

Details: Pharma companies have always concentrated on building systems for quality - conscious drug manufacturing. At a foreign regulatory audit, however, it is not only the company image that is projected; it is also the professional culture as well as knowledge base that leave a lasting impact. In spite of facing many regulatory inspections, Pharma companies still lack finesse, detailed preparedness and a systematic approach while facing most regulatory inspections.

For this program, our industry expert, Maija Heitava – Lorenzi will share her experience and expertise as a Regulator and Inspector, as well as provide valuable inputs on the Do’s and Don’ts of an audit. Whether it is a self-audit or whether it is the EU, USFDA or MHRA, this course provides practical points on getting it right the first time, every time.

for more info visit:www.pharmasupport.in

Get registration for this event visit: pharma-event-registration