If you wish to register more than one individual, use the multiple registrants form.

If you prefer credit card payment (Visa, MC or AmEx), please use our PDF form
and fax the signed registration to us.

Fill out the form and click the "Register" button to complete your registration.
A confirmation will be sent to you by fax or e-mail within a week.

Swedish customers can be invoiced in SEK if specified in registration.
The price is then calculated from the the current exchange rate at the invoice date.

Prices for courses more than 6 month in the future are preliminary and can be subjected
to changes.

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The course fee will be excluded VAT for participants coming from countries outside EU, and for participants from registered companies within EU, excluding Swedish participants where a 25% VAT will be added. For statistical tax reporting of trade between EU countries, information of company VAT no. is mandatory and we therefore ask you to fill in the above, if applicable.

Mark the courses you wish to attend:

Click the titles for full course description, instructors and pricing

Batch Record Review and Investigations (Code 5301)
	1-3 June, 2009   Prague, Czech republic
Basic Statistics in QC-lab environment, On-line  (Code 5901)
	On -line course, please register on » separate form
CGMP: Interpretation and Application (Code 5302)
	27-29 May, 2009   Prague, Czech republic
Compliance for Biopharmaceutical API Process Validation (Code 5213)
	1-3 June, 2009   Prague, Czech republic
Compliance to Clinical Safety and Pharmacovigilance Regulations (Code 5217)
	4-5 June, 2009   Prague, Czech republic
Design Control Requirements and Industry Practice (Code 5307)
	21-23 October, 2009  Copenhagen, Denmark
GMP Compliance Auditing  (Code 5201)
	19-20 October, 2009  Copenhagen, Denmark
GMP Compliance and Auditing for Sterile Pharmaceuticals (Code 5303)
	21-23 October, 2009  Copenhagen, Denmark
GMP Compliance for Quality Control and Laboratory Operation (Code 5202)
	26-27 October, 2009  Copenhagen, Denmark
Practical Approaches to Global GMP for Investigational Materials (Clinical Trial Materials) (Code 5209)
	4-5 June, 2009   Prague, Czech republic
Understand ICH Q8/Q9/Q10 in your GMP environment (Code 5106)
	4 May, 2009  Copenhagen, Denmark
Validation and Qualification Compliance Requirements  (Code 5206)
	25-26 May, 2009   Prague, Czech republic
Quality System Requirements and Industry Practice (Code 5501)
	25-29 May, 2009   Prague, Czech republic