Workshops
“Evaluations take too long, everyone on the team evaluates differently, and in the audit the traceable path to the result is missing.”
Evaluate faster. Document audit-proof.
Two workshops for analytical, QC and CMC teams, both with one goal: your team evaluates faster, and every number stands up to inspection. Always on real data, in-house on your own.
30 minutes on Microsoft Teams with the CovaSyn team. If it is not a fit, we will say so.
- November 2026
- Audit-proof GMP labhalf day
- December 2026
- Faster evaluation in R&Dtwo days
- January 2027
- Structure elucidationtwo days
- Audit-proof GMP labhalf day
- February 2027
- Stability per ICH Q1two days
- ICH M7 in silicotwo days
If nothing changes
What it costs when everyone evaluates differently.
- Everyone tries something different, and the results cannot be compared.
- In the audit nobody can recalculate how a number came about, and the rework costs days.
- The one expert becomes the bottleneck, and every evaluation waits for them.
How we help
How our workshops work.
On real cases instead of slides, with a finished evaluation path to take home. Fixed dates, open prices, bookable online.
- Save time
- Your team learns in one session what would otherwise take months of trial and error.
- Save costs
- Less rework after the audit and less waiting for the one expert.
Evidence
Measured, not claimed.
- Without CovaSyn
- 14 to 41%
- With CovaSyn
- 76 to 92%
Workshop 1
Evaluation in the GMP lab: faster and audit-proof
An evaluation that nobody can recalculate in an audit costs days of rework. On a real case, your team learns to evaluate spectra, stability and impurity data faster and to document them so that every calculation step stands up to an inspection.
- For whom
- QA, QC, analytical, validation and lab leadership in pharma, CDMOs and chemistry
- Formats
- Online compact and in-house
- 01Where evaluations in the regulated lab cost time today and are open to challenge in an audit
- 02The regulatory framework at a glance: Annex 11, data integrity under ALCOA+, GAMP 5 (orientation, not advice)
- 03Computing reproducibly: same data, same result, every calculation step documented
- 04Your case: one real evaluation step by step, from raw data to sign-off by the expert
- 05Exercise: inventory your own evaluations and classify them by criticality
- 06Roadmap: what the lab can put in place now
This content is not legal, regulatory or compliance advice.
Workshop 2
Specialist workshop on your lab problem
One problem, two days, one result. Your team works on its own data and leaves with a verified evaluation path that holds up in the lab the next morning.
Faster evaluation in research and development
Two days on your own questions: literature, structure proposals, evaluation, documentation. You leave with a workflow, not a demo.
Faster structure elucidation: NMR, MS, IR and UV/Vis
Spectra interpretation, purity assessment and impurity identification, each computed reproducibly. The focus is on when you may trust a proposal and when you may not.
Stability under ICH Q1: Arrhenius, shelf life and OOS/OOT
Turning multi-temperature data into a defensible shelf-life estimate, justifying model selection, and recognising when extrapolation cannot replace the real-time study.
ICH M7 in silico: mutagenic impurities and expert review
Structural alert triage, class 1 to 5 classification, and handling two complementary systems that disagree. With a traceable audit trail.
Your own topic
Method transfer, mass balance, an unknown peak: we build the workshop around the problem holding up your lab right now, as an in-house date.
Open dates
Choose a date and book directly.
Every date can be booked on its own, in Leipzig or online. You can pay online or on invoice with your purchase order number (short email to support@covasyn.com). The confirmation with a calendar entry arrives by email.
19 Nov 2026
Half day online (9am to 1pm)online
Evaluation in the GMP lab: faster and audit-proof
Half a day on real cases from the regulated lab. You see where evaluations lose days today, what a result looks like that any inspection can recalculate, and what your team starts with tomorrow.
Method
- Where evaluations in the regulated lab cost time today and are open to challenge in an audit
- Data integrity under ALCOA+, audit trail and method validation at a glance
Hands-on with your data
- One real case step by step, from raw data to sign-off by the expert
- Roadmap: what your lab can put in place right away
Included:MaterialsRecording€490
per person excl. VAT
1 and 2 Dec 2026
Two days, 20 teaching units (9am to 6pm)Marriott Leipzig or online
Faster evaluation in research and development
Two days on your own questions: literature, structure proposals, evaluation, documentation. You leave with a workflow, not a demo.
Method
- Question, data basis, limits, checking results
- Documenting literature work and structure proposals traceably
Hands-on with your data
- Your own molecules and questions, evaluated step by step
- Your own use case on day two, supervised
Included:MaterialsCertificate30-day follow-up€1,490
per person excl. VAT
19 and 20 Jan 2027
Two-day intensive workshop (9am to 6pm)Marriott Leipzig
Faster structure elucidation: NMR, MS, IR and UV/Vis
Spectra interpretation, purity assessment and impurity identification, each computed reproducibly. The focus is on when you may trust a proposal and when you may not.
Method
- Signal assignment, confidence and applicability domain
- When a structure verification holds up and when it is guessing
Hands-on with your data
- Your own spectra, from assignment to report
- Templates for assignment and purity assessment
Included:MaterialsCateringCertificate30-day follow-up€1,790
per person excl. VAT
28 Jan 2027
Half day online (9am to 1pm)online
Evaluation in the GMP lab: faster and audit-proof
Half a day on real cases from the regulated lab. You see where evaluations lose days today, what a result looks like that any inspection can recalculate, and what your team starts with tomorrow.
Method
- Where evaluations in the regulated lab cost time today and are open to challenge in an audit
- Data integrity under ALCOA+, audit trail and method validation at a glance
Hands-on with your data
- One real case step by step, from raw data to sign-off by the expert
- Roadmap: what your lab can put in place right away
Included:MaterialsRecording€490
per person excl. VAT
9 and 10 Feb 2027
Two days, 20 teaching units (9am to 6pm)Marriott Leipzig or online
Stability under ICH Q1: Arrhenius, shelf life and OOS/OOT
Turning multi-temperature data into a defensible shelf-life estimate, justifying model selection, and recognising when extrapolation cannot replace the real-time study.
Method
- Kinetics, Arrhenius, model selection by AIC, poolability
- OOS and OOT detection, significant change, residual diagnostics
Hands-on with your data
- Your own or supplied data sets
- Documenting the limits of extrapolation properly
Included:MaterialsCertificate30-day follow-up€1,490
per person excl. VAT
23 and 24 Feb 2027
Two-day intensive workshop (9am to 6pm)Marriott Leipzig
ICH M7 in silico: mutagenic impurities and expert review
Structural alert triage, class 1 to 5 classification, and handling two complementary systems that disagree. With a traceable audit trail.
Method
- (Q)SAR, applicability domain, expert review under ICH M7
- Resolving contradictory predictions from two systems with justification
Hands-on with your data
- Assess entire impurity lists in one pass
- First-pass report templates (FDA, EMA)
Included:MaterialsCateringCertificate90-day follow-up€1,790
per person excl. VAT
Planning for a team?
For two days, an in-house date costs less than individual seats from 7 people in one organisation, for a half day from 8. On your own use case and on a date of your choice.
A free way in before a workshop: the CovaSyn Open Lab, 45 minutes live on Microsoft Teams once a month.
FAQ
Frequently asked questions
Who are the workshops for?
For analytical, QC, CMC, QA and lab leadership in pharma, CDMOs and chemistry. Workshop 1 is for the regulated lab, workshop 2 for any team with a concrete evaluation problem.
Are there in-house dates?
Yes. You book in-house formats for your team. Formats and prices are in the catalogue.
How do I book?
Online, right in the catalogue, or on invoice with your purchase order number: a short email to support@covasyn.com is all it takes. The confirmation with a calendar entry arrives by email.
How reliable are the results?
14 to 41% without CovaSyn, 76 to 92% with CovaSyn. Measured on MolecularIQ, an independent benchmark we did not design (ICLR 2026, arXiv:2601.15279, Klambauer Lab, JKU Linz). Every result comes as a reasoned report that your expert reviews and releases.
When is an in-house date worth it?
For two days, an in-house date costs less than individual seats from 7 people in one organisation, for a half day from 8. On your own use case and on a date of your choice.
What if no open date suits us?
New open dates appear in the catalogue as soon as they are set. An in-house date for your team can be planned independently of that, on a date of your choice.
Next step
Give your team a shared starting point.
Open dates at a fixed price, bookable online. Or in-house, on a case from your own lab.