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Machinery & Technology

From batch to flow: continuous manufacturing and what it means for tablet plants

Regulators now have a global guideline, and continuous lines have shortened release times and approvals. Where the technology stands.

From batch to flow: continuous manufacturing and what it means for tablet plants
In this article
  1. The milestones
  2. What it has delivered
  3. The global rulebook
  4. The barriers
  5. How a continuous line works
  6. Batch and continuous compared
  7. Where it fits best
  8. Questions to ask before investing
  9. What it means for Pakistan
  10. Sources

Most medicines are still made in batches: a quantity of powder is blended, granulated, dried, compressed and coated, step by step, with tests and waiting in between. Continuous manufacturing links those steps into one flowing line, monitored as it runs.

The milestones

YearMilestone
2015Vertex’s Orkambi becomes the first FDA approval made by continuous manufacturing
2016FDA allows Janssen to switch Prezista (darunavir) from batch to continuous — the first such switch
2020FDA approves four drugs made by continuous manufacturing
November 2022ICH adopts guideline Q13 on continuous manufacturing of drug substances and products

Other approved examples include Vertex’s Symdeko and Trikafta, Pfizer’s Daurismo and Eli Lilly’s Verzenio.

What it has delivered

  • Janssen said its switch reduced testing-to-release time from 30 days to a target of 10 days.
  • An FDA self-audit in 2022 found continuous-manufacturing applications were approved in the first review cycle, about nine months faster than comparable batch applications against target, and reached the market 12 months faster after submission.
  • FDA lists benefits including less manual handling, online quality monitoring, smaller equipment and space, and faster response to shortages.

The global rulebook

ICH Q13 covers both active ingredients and finished products and explains that continuous processes still produce defined batches, set by quantity or run time. It applies to new products and to converting existing batch processes.

The barriers

The industry’s installed base is still batch, and moving requires investment in equipment, process analytical technology (PAT) and training. Changing an approved product also needs regulatory change control.

How a continuous line works

In a continuous tablet line, ingredients are fed by gravimetric feeders at precisely controlled rates into a continuous blender. The blend flows on to granulation (or straight to compression in a direct-compression process), then to the tablet press and coater, without stopping between steps. Sensors along the line — often near-infrared spectroscopy and other process analytical technology (PAT) — measure the blend and the product as it moves, and a control system adjusts the process in real time.

Because material moves constantly, two ideas become important:

  • Residence time distribution — how long material spends in each unit. It tells the manufacturer which tablets came from which raw material lot, which is essential for traceability.
  • Diversion — if a sensor detects material outside specification, the system automatically diverts the affected portion so that only good product continues.

Batch and continuous compared

BatchContinuous
Quality testingMainly at the end of each stepContinuous monitoring during production
Scale-upLarger equipment, repeated developmentRun longer on the same equipment
FootprintSeveral rooms and hold stepsA compact, connected line
Skills neededEstablished and widely availableProcess control, data and PAT expertise

Where it fits best

Continuous manufacturing suits high-volume products made for long periods, products whose demand changes and must be scaled quickly, and new products developed with the approach in mind. It is less attractive for small-volume products that share equipment with many others. That is why most companies start with one product, often a new one, rather than converting an entire plant.

Questions to ask before investing

  1. Which products have the volume and lifetime to justify a dedicated continuous line?
  2. Do we have, or can we hire, people with process-control and data skills?
  3. Which regulators will review the change, and what data will they expect?
  4. Can parts of the approach — inline monitoring, automated feeding — improve our batch lines first?

Asking these questions early helps a company choose the right first project and avoid buying technology it is not yet ready to run.

What it means for Pakistan

Few plants will switch overnight, but the building blocks — inline monitoring, automation, data systems — pay off in batch plants too, and matter for export-grade quality. Machinery suppliers show these technologies at Pharma Asia 2026; see also AI and digital twins.

Sources