Simple EP 2.2.48 Compliance

On April 1, 2016, a revision to European Pharmacopoeia (EP) Supplement 8.7, Chapter 2.2.48 takes effect. This revision establishes new standards, specifically acceptable tolerances for handheld Raman instrumentation.

With the increased implementation of handheld Raman analyzers for streamlining workflow requirements, Pharmaceutical manufacturers now have set guidance for instrumentation performance.

It’s a great time to upgrade your handheld Raman!

Do you have an older generation handheld Raman? With the new standards, now is a great time to upgrade! Take advantage of this opportunity to easily implement Progeny 1064nm handheld Raman into your workflow process.

Validate the largest number of your materials. User customizable IQOQPQ and SOP packages make upgrading easier than ever! Stop supporting outdated handheld Raman technology that may be discontinued in the near future. Save time and money with the most advanced 1064nm handheld Raman available. Ask us about our generous trade-in discounts today!

Progeny 1064nm handheld Raman User Compliance

Rigaku Analytical Devices is committed to exceeding our customer’s expectations. Our team is at the forefront of current and upcoming regulatory requirements effecting our customers’ utilization of handheld Raman devices within each individual industry they serve. Our team has been working diligently to ensure Progeny’s compliance with EP 2.2.48 standards. Completion of an update and validation procedures will be available prior to or on the April 1, 2016 effective date.

All customers will receive notification.

Progeny 1064nm handheld Raman spectrometer remains the instrument of choice for rapid, accurate and reliable complete identification of the largest number of pharmaceutical raw materials and finished products.

To request a copy of our European Pharmacopoeia Supplement 8.7 Chapter 2.2.48 State of Compliance, request more information or submit updated contact information specific to your Progeny unit, please select this link.

For more information on EP Supplement 8.7, select this link.
Progeny 1064nm handheld Raman european pharmacopoeia regulatory compliance image European pharmacopoeia 8th edition regulations Progeny handheld Raman compliance documents thumbnail

Simple EP 2.2.48 Compliance

On April 1, 2016, a revision to European Pharmacopoeia (EP) Supplement 8.7, Chapter 2.2.48 takes effect. This revision establishes new standards, specifically acceptable tolerances for handheld Raman instrumentation.

With the increased implementation of handheld Raman analyzers for streamlining workflow requirements, Pharmaceutical manufacturers now have set guidance for instrumentation performance.

It’s a great time to upgrade your handheld Raman!

Do you have an older generation handheld Raman? With the new standards, now is a great time to upgrade! Take advantage of this opportunity to easily implement Progeny 1064nm handheld Raman into your workflow process.

Validate the largest number of your materials. User customizable IQOQPQ and SOP packages make upgrading easier than ever! Stop supporting outdated handheld Raman technology that may be discontinued in the near future. Save time and money with the most advanced 1064nm handheld Raman available. Ask us about our generous trade-in discounts today!

Progeny 1064nm handheld Raman User Compliance

Rigaku Analytical Devices is committed to exceeding our customer’s expectations. Our team is at the forefront of current and upcoming regulatory requirements effecting our customers’ utilization of handheld Raman devices within each individual industry they serve. Our team has been working diligently to ensure Progeny’s compliance with EP 2.2.48 standards. Completion of an update and validation procedures will be available prior to or on the April 1, 2016 effective date.

All customers will receive notification.

Progeny 1064nm handheld Raman spectrometer remains the instrument of choice for rapid, accurate and reliable complete identification of the largest number of pharmaceutical raw materials and finished products.

To request a copy of our European Pharmacopoeia Supplement 8.7 Chapter 2.2.48 State of Compliance, request more information or submit updated contact information specific to your Progeny unit, please select this link.

For more information on EP Supplement 8.7, select this link.
Progeny 1064nm handheld Raman european pharmacopoeia regulatory compliance image European pharmacopoeia 8th edition regulations Progeny handheld Raman compliance documents thumbnail

Simple EP 2.2.48 Compliance

On April 1, 2016, a revision to European Pharmacopoeia (EP) Supplement 8.7, Chapter 2.2.48 takes effect. This revision establishes new standards, specifically acceptable tolerances for handheld Raman instrumentation.

With the increased implementation of handheld Raman analyzers for streamlining workflow requirements, Pharmaceutical manufacturers now have set guidance for instrumentation performance.

It’s a great time to upgrade your handheld Raman!

Do you have an older generation handheld Raman? With the new standards, now is a great time to upgrade! Take advantage of this opportunity to easily implement Progeny 1064nm handheld Raman into your workflow process.

Validate the largest number of your materials. User customizable IQOQPQ and SOP packages make upgrading easier than ever! Stop supporting outdated handheld Raman technology that may be discontinued in the near future. Save time and money with the most advanced 1064nm handheld Raman available. Ask us about our generous trade-in discounts today!

Progeny 1064nm handheld Raman User Compliance

Rigaku Analytical Devices is committed to exceeding our customer’s expectations. Our team is at the forefront of current and upcoming regulatory requirements effecting our customers’ utilization of handheld Raman devices within each individual industry they serve. Our team has been working diligently to ensure Progeny’s compliance with EP 2.2.48 standards. Completion of an update and validation procedures will be available prior to or on the April 1, 2016 effective date.

All customers will receive notification.

Progeny 1064nm handheld Raman spectrometer remains the instrument of choice for rapid, accurate and reliable complete identification of the largest number of pharmaceutical raw materials and finished products.

To request a copy of our European Pharmacopoeia Supplement 8.7 Chapter 2.2.48 State of Compliance, request more information or submit updated contact information specific to your Progeny unit, please select this link.

For more information on EP Supplement 8.7, select this link.

Progeny 1064nm handheld Raman european pharmacopoeia regulatory compliance image
European pharmacopoeia 8th edition regulations Progeny handheld Raman compliance documents thumbnail